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Hitachi CXR4 Computed Tomography Scanner. This product is an x-ray imaging device that produces cross-sectional images of he body at different angles. The system reconstructs, processes, displays, and stores the collected images. The device output can provide an aid to diagnosis when used by a qualified physician and is intended for general purpose CT applications.

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code JAK·November 5, 2008

Hitachi CXR-4 CT Computed Tomography X-ray System (including SceptreP3 PET/CT)

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code JAK·February 21, 2006

Hitachi Emission Computed Tomography System Hitachi CX-4 CT (including SceptreP3 PET-CT)

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code JAK·February 21, 2006

ECAT Emerge PET Scanners (distributed by Siemens Medical Solutions USA, Inc.), ECAT ART PET Scanners (distributed by Siemens Medical Solutions USA, Inc.) and Sceptre PET Scanners (distributed by Hitachi Medical Systems of America)

FDA Recall
Terminated ·Siemens Medical Solutions USA Inc·Product code KPS·March 28, 2006

ECAT PET Scanners (mobile systems), distributed by Siemens Medical Solutions ECAT PET Scanners (mobile systems), and Reveal XL (mobile systems), distributed by CTI Molecular Imagining, Inc. Sceptre and Sceptre XL (mobile systems) distributed by Hitachi Medical Systems America

FDA Recall
Terminated ·CTI PET Systems Inc·Product code KPS·April 5, 2005

EUB-5500 VISION 5500 Diagnostic Ultrasound Scanner w/Step 5 (V05-7) Software. Imaging device intended to provide the physician with physiological and clinical information.

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code LHN·February 25, 2008

Hitachi Scenaria CT System Software Product Usage: The Scenaria system is indicated to acquire axial volumes of the whole body including the head. The images can be acquired in either axial, helical, gated or dynamic modes. The volume datasets acquired by the Scenaria can be post processed by the Scenaria to provide additional information. Post processing capabilities included in the Scenaria software include CT angiography (CTA), Multi-planar reconstruction (MPR) and volume rendering.

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code JAK·May 4, 2012

Hitachi HI VISION 6500, Model #EUB-6500, Ultrasound Diagnostic Scanner Device, Software Version V04-04 DICOM ServicePack 1 and EZU-FC5W.

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code ITX·May 7, 2004

Hitachi AIRIS, AIRIS II, AIRIS Elite MRI Scanner Compensation Coil. Part numbers: MR-FC-2EO, MR-FC-3EO

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code MOS·April 19, 2010

Magnetic Resonance Imaging Device

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code LNH·February 21, 2006

EUB-9500/HI VISION 8500 Diagnostic Ultrasound Scanners, DICOM Option EZU-FC6, Software Versions: V11-01, V11-03, V12-03 and V12-04A.

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code ITX·May 12, 2008

Hitachi Echelon MRI System/Oasis MRI, Software. These are software controlled MRI devices. Product Usage: The Echelon and Oasis MR systems are imaging devices, intended to provide the physician with physiological and clinical information that can be useful in diagnosis determination.

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code LNH·June 15, 2012

Hitachi Altaire Magnetic Resonance Imaging System

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code LNH·January 27, 2006

EUB-6500/HI VISION 6500 Diagnostic Ultrasound Scanners, DICOM Option EZU-FC5, Software Versions: V01-03, V01-05, V02-04, V03-02, V04-02, V04-03, V04-04, V05-03, V05-05A, V05-07A and V05-30A.

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code ITX·May 12, 2008

Echelon, Echelon Oval and Oasis MR imaging device systems; one unit per box. The Echelon, Echelon Oval and Oasis MR systems are imaging devices, and are intended to provide the physician with physiological and clinical information, obtained non-invasively and without the use of ionizing radiation. The MR systems produce transverse, coronal, sagittal, oblique, and curved cross-sectional images that display the internal structure of the head, body, or extremities.

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code LNH·January 31, 2013

Hitachi Oasis MRI system Product Usage: Hitachi MR system is an imaging device and is intended to provide the physician with physiological and clinical information, obtained non-invasively and without the use of ionizing radiation. The Oasis system produces transverse, coronal, sagittal, oblique, and curved crosssectional images that display the internal structure of the head, body, or extremities. The images produced by the MR systems reflect the spatial distribution of protons (hydrogen nuclei) exhibiting magnetic resonance. The NMR properties that determine the image appearance are proton density, spin-lattice relaxation time (T1), spin-spin relaxation time (T2), and flow. When interpreted by a trained physician, these images provide information that can be useful in diagnosis determination.

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code LNH·June 18, 2018

Hitachi Scenaria CT system Product Usage: The SCENARIA CT system is indicated for head, whole body, cardiac and vascular X-ray Computed Tomography applications in patients of all ages. The images can be acquired in either axial, helical, gated or dynamic modes. The volume datasets acquired by the SCENARIA can be post processed by the SCENARIA to provide additional information. Post processing capabilities included in the SCENARIA software include CT angiography (CTA), Multiplanar reconstruction (MPR) and volume rendering. Volume datasets acquired by the SCENARIA Phase 3 can be transferred to external devices via a DICOM standard interface. The guideShot Option adds a remote in-room display and controls to support interventional imaging. The device output can provide an aid to diagnosis when used by a qualified physician.

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code JAK·June 29, 2018

Hitachi Echelon Oval MRI System

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code LNH·April 16, 2015

Hitachi Oasis MRI System

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code LNH·April 16, 2015

Hitachi HIVISION Preirus/Avius Ultrasound equipped with V03.02 Software - Doppler Trace Measurement program. 510 (k) Numbers: Preirus - K093466 (6/1/10), Avius - K102901 (10/27/10). The Preirus and Avius are intended for use by trained personnel (doctors, sonographers, etc) for the diagnostic ultrasound evaluation of Abdominal, Cardiac, Intra-operative, Feta, Pediatric, Small Organ, Peripheral vessel, Biopsy, Trans-rectal, Trans-vaginal, Musculoskeletal, Neonatal Cephalic, Adult Cephalic, Endoscopy, Intra-luminal, Genecology, Urology and Laparoscopic clinic applications. The Modes of Operation of the HIVISION Preirus are B mode, M mode PW mode (Pulsed Wave Doppler), CW mode (Continuous Wave Doppler) Color Doppler, Amplitude Doppler (Color Flow Angiography), TDI (Tissue Doppler Imaging), 3D Imaging, 4D Imaging, RealTime Tissue Elastography, and Real Time Virtual Sonography.

FDA Recall
Terminated ·Hitachi Medical Systems America Inc·Product code IYN·April 18, 2011