8 results
·
26ms
·
Sources: EU EUDAMED, US FDA
MODELS 3987 AND 3988 RESUME LEAD FOR PNS
FDA 510(k)
FDA Class 2
·Neurology
AKUPORT M1
FDA 510(k)
FDA Class 2
·Neurology
GYRUS AMCI PK BUTTON ELECTRODE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BONE SCREW 6,5 H.30MM
FDA Adverse Event
Malfunction
·LIMACORPORATE S.P.A.·Product code LPH·May 5, 2020
MEDFUSION 3500
FDA Adverse Event
Injury
·SMITHS MEDICAL·Product code FRN·November 17, 2010
ACCENT DR RF
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·July 8, 2014
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·December 7, 2012
BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal specimens Catalog Number: 444213
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Co.·April 21, 2021