6 results
·
18ms
·
Sources: EU EUDAMED, US FDA
VOYAGR SERIES DIAGNOSTIC EP CATHETERS
FDA 510(k)
FDA Class 2
·Cardiovascular
BMR NEUROTECH BACK TENS AND LUMBAR SUPPORT DEVICE. TYPE 294
FDA 510(k)
FDA Class 2
·Neurology
PSA SERIES
FDA 510(k)
FDA Class 2
·Cardiovascular
ANIMAS INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·ANIMAS CORP.·Product code LZG·December 13, 2010
1.8MM TI LOCKING SCREW
FDA Adverse Event
Injury
·SYNTHES USA·Product code MNI·January 22, 2013
QUARTET
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code OJX·July 9, 2014