8 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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AGE Automatic Upper Arm Blood Pressure Monitor with models BA-815, BA-816, BA-818 and BA-819
FDA 510(k)
FDA Class 2
·Cardiovascular
WMT IMPLANTABLE K-WIRE
FDA 510(k)
FDA Class 2
·Orthopedic
ONE DAY FLAT PACK
FDA 510(k)
FDA Class 2
·Ophthalmic
PINNACLE MTL INS NEUT36IDX54OD
FDA Adverse Event
Injury
·8010379 DEPUY INTL., LTD.·Product code KWA·June 17, 2013
VITALITY 2
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 22, 2011
BRAVO
FDA Adverse Event
Malfunction
·ARIZONA DEVICE MANUFACTURING·Product code FFT·September 19, 2008
WILSON-COOK ACHALASIA BALLOON
FDA Adverse Event
Injury
·COOK ENDOSCOPY·Product code PID·June 17, 2021
WILSON-COOK ACHALASIA BALLOON
FDA Adverse Event
Malfunction
·COOK ENDOSCOPY·Product code PID·October 6, 2020