8 results · 26ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

DMA MICROPROTEIN PROCEDURE

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

GENERATOR, 16 SERIES, MODIFIED TOP CAP

FDA 510(k)
FDA Class 3 ·Cardiovascular

Cleerly Labs

FDA 510(k)
FDA Class 2 ·Radiology

WISP MASK, FABRIC FRAME

FDA Adverse Event
Injury ·RESPIRONICS INC.·Product code BZD·June 4, 2014

GREENLIGHT ADDSTAT

FDA Adverse Event
Malfunction ·AMS , INNOVATION CTR - SILICON VALLEY·Product code GEX·October 28, 2010

LIFEVEST WCD 4000 SYSTEM

FDA Adverse Event
Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·November 21, 2012

GE HC OEC 9900 Elite and GE OEC 9800 Fluoroscopes Snubber Boards are a PCB with a 70 amp fuse to provide fused protection of internal system components from the high voltage system components, such as the X-ray tube or High Voltage Transformer. System model number A349855, Snubber Board number 00-880405-03 rev 5. This product is used for image intensified fluoroscopic x-rays for interventional radiologic procedures.

FDA Enforcement
Class II ·Terminated·GE OEC Medical Systems, Inc·August 29, 2012

OEC 9800; OEC FluoroTrak 9800 Plus; OEC 9800 Plus; OEC 9800 MD Motorized C-arm System, 892.1650 Image-intensified fluoroscopic x-ray system. The OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. The system includes features specifically designed for use in diagnostic and interventional cardiac imaging procedures and is also intended for cholangiography, endoscopic, urologic orthopedic, neurologic, vascular, critical care and emergency room procedures. It may be used for other imaging applications at the physician's discretion.

FDA Enforcement
Class I ·Terminated·GE OEC Medical Systems, Inc·August 1, 2012