8 results
·
27ms
·
Sources: EU EUDAMED, US FDA
PHILIPS BV 300 SERIES
FDA 510(k)
FDA Class 2
·Radiology
NA
FDA UDI
SCHÖLLY FIBEROPTIC GmbH·04250480107614·Controller Full HD
LUBRICATING JELLY
FDA 510(k)
FDA Class 1
·General Hospital
SUTURE REMOVAL KIT
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·January 14, 2013
LIFEPAK 20 DEFIBRILLATOR/MONITOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code LDD·December 15, 2010
TENDRIL ST
FDA Adverse Event
Death
·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 23, 2014
Vanguard XP Tibial Tray 67 mm Item # 195247
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·September 18, 2019