6 results
·
21ms
·
Sources: EU EUDAMED, US FDA
IMPERVA-A
FDA 510(k)
FDA Class 2
·Dental
BIS MODULE FOR ENVOY PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Neurology
Revitalair 430F
FDA 510(k)
FDA Class 2
·Anesthesiology
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 17, 2014
UNKNOWN LEFT HIP REJUVENATE/ ABGII STEM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·December 6, 2012
FLEXTEND
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·October 16, 2010