7 results
·
34ms
·
Sources: EU EUDAMED, US FDA
STANICOR THETA MODEL 221 CARDIAC PACER
FDA 510(k)
FDA Class 3
·Cardiovascular
3030677-2018-02479
FDA Adverse Event
Malfunction
·November 5, 2018
Bio-Medicus Adult Cannulae and Introducer
FDA 510(k)
FDA Class 2
·Cardiovascular
REGULATOR, PRESSURE, CUFF
FDA 510(k)
FDA Class 2
·Anesthesiology
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORP·Product code FRN·January 7, 2014
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·October 10, 2012
FREESTYLE FLASH
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE INC, USA·Product code LFR·July 16, 2007