6 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MODIFIED USE FOR MODEL 6110A IONTOPHORETIC APPLI.
FDA 510(k)
FDA Class 2
·Physical Medicine
TENS/IF 14
FDA 510(k)
FDA Class 2
·Neurology
Sutter CURIS RF Generator
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 13, 2014
RENAL - DISPOSABLE
FDA Adverse Event
Injury
·Product code KDJ·October 16, 2010
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·December 13, 2012