6 results
·
17ms
·
Sources: EU EUDAMED, US FDA
BACKHAUS CLAMP, 5 1/4
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
ARTERIA BLOOD FILTER
FDA 510(k)
FDA Class 2
·General Hospital
CS-SERIES-FP WITH 3030+OPTION
FDA 510(k)
FDA Class 2
·Radiology
2600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 16, 2014
PULSAR GENERATOR
FDA Adverse Event
Malfunction
·MEDTRONIC ADVANCED ENERGY LLC·Product code GEI·October 25, 2012
POSEY SEAT BELT SENSOR
FDA Adverse Event
Malfunction
·DONGGUAN POSEY MEDICAL DEVICE LTD.·Product code KMI·August 26, 2010