7 results
·
22ms
·
Sources: EU EUDAMED, US FDA
KING KRIB
FDA 510(k)
FDA Class 1
·General Hospital
EURO-DIAGNOSTIC BLOOD PRESSURE MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
UNICONDYLAR FIBER METAL KNEE
FDA 510(k)
FDA Class 2
·Orthopedic
OCTRODE
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 7, 2013
ROTOPRONE THERAPY SYSTEM
FDA Adverse Event
Malfunction
·KCI USA, INC.·Product code IKZ·November 24, 2010
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 1, 2014
Presource PBDS, Total Knee, Kit, Circulator
FDA Enforcement
Class I
·Terminated·Cardinal Health, Medical Products & Services·May 15, 2013