6 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GUIDE WIRES, MODIFICATION
FDA 510(k)
FDA Class 2
·Cardiovascular
HOFFMANN DYNAMIC WRIST FIXATOR
FDA 510(k)
FDA Class 2
·Orthopedic
PROGRAMMABLE VIDEO CONTROLLER MODEL PK2060
FDA 510(k)
FDA Class 2
·Radiology
PROLIFT PELVIC FLOOR REPAIR
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·November 30, 2010
OT VERIO PRO METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 6, 2014
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 20, 2012