6 results
·
35ms
·
Sources: EU EUDAMED, US FDA
AGRAM SPYRAL ELECTRODE
FDA 510(k)
FDA Class 2
·Neurology
ALGINATE FIBER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
BUTTON REPLACEMENT GASTROSTOMY DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
UNKNOWN DEPUY FEMORAL STEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWA·January 30, 2013
FREESTYLE LITE
FDA Adverse Event
Injury
·Product code NBW·December 21, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 4, 2014