8 results
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26ms
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Sources: EU EUDAMED, US FDA
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