6 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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308nm Excimer Phototherapy Device (CN-308E, KN-4003B3, KN-4003B4, KN-5000C KN-5000D, KN-5000H, KN-5000K)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Alinity m STI Assay
FDA 510(k)
FDA Class 2
·Microbiology
LASIK EYE DRAPE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
6F ANGIO-SEAL VASCULAR CLOSURE DEVICE STS PLUS
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code MGB·November 20, 2008
RIATA ACTIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 11, 2011
OT VERIO IQ METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013