6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Resectr Tissue Resection Device
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
PRESSURE RELEASE VALVE W/AUDIBLE, MODEL PRV 20/40/60; WITH T6 ADAPTER, MODEL PRV 120/140/160; T6 ADAPTER, MODEL T6-100
FDA 510(k)
FDA Class 2
·Anesthesiology
HANDHELD MANUAL BREAST PUMP (AVENT MANUAL BREAST PUMP)
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·June 26, 2013
ENDEAVOR SPRINT RX CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code NIQ·July 20, 2011
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·September 26, 2008