8 results · 19ms · Sources: EU EUDAMED, US FDA

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ESPE CAPMIX

FDA 510(k)
FDA Class 1 ·Dental

Argon Handset

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

NAVILAS LASER SYSTEM

FDA 510(k)
FDA Class 2 ·Ophthalmic

INFINITI VISION SYSTEM OZIL

FDA Adverse Event
Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·October 29, 2010

SPECTRUM INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 31, 2014

MAXPLUS CLEAR NEEDLELESS CONNECTOR

FDA Adverse Event
Malfunction ·CAREFUSION CORP.·Product code FPA·November 14, 2012

DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE, E-MINIC AND ACCESSORIES. DATEX-OHMEDA S/5TM FM WITH L-FICU04 ANDL-FICUO4A SOFTWARE AND N-FCREC MODULE **(OUS only). E-miniC and accessories is indicated for monitoring C02 and respiration rate of all hospital patients.

FDA Enforcement
Class I ·Terminated·GE Healthcare, LLC·July 30, 2014

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