7 results
·
33ms
·
Sources: EU EUDAMED, US FDA
BONE MARROW BIOPSY DEVICE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
X-RAY DIAG. TABLE DT-KCS
FDA 510(k)
FDA Class 2
·Radiology
FOSSA URETERAL OPEN STENTS
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
RENAL UROLOGY STENT K072293
FDA Adverse Event
Other
·FOSSA MEDICAL INC·Product code FAD·April 10, 2014
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·October 4, 2012
LIBERTY CYCLER
FDA Adverse Event
Malfunction
·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FKX·December 19, 2013
PFC SIG RPF INS SZ 3 10MM
FDA Adverse Event
Injury
·DEPUY-RAYNHAM, A DIV. OF DEPUY ORTHOPAEDICS·Product code NJL·July 22, 2010