6 results
·
32ms
·
Sources: EU EUDAMED, US FDA
BURTON RADIUSGAUGE - MODEL 2030
FDA 510(k)
FDA Class 1
·Ophthalmic
CRI CYNOSAR CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
WHEELCHARIOT LIGHTWEIGHT MANUAL WHEELCHAIR
FDA 510(k)
FDA Class 1
·Physical Medicine
COULTER AC*T DIFF 2 ANALYZER
FDA Adverse Event
Injury
·BECKMAN COULTER, INC.·Product code GKZ·January 22, 2013
INTERSTIM II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUCNOS·Product code EZW·December 7, 2010
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·July 10, 2014