6 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PHORESOR II,MODEL PM900
FDA 510(k)
FDA Class 2
·Physical Medicine
BIO-SCREEN
FDA 510(k)
FDA Class 2
·Dental
Rapid Reboot Compression Therapy System
FDA 510(k)
FDA Class 2
·Physical Medicine
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·June 16, 2014
HUDSON CONCHATHERM NEPTUNE
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BZE·February 25, 2013
NC QUANTUM APEX PTCA DILATATION CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·February 9, 2011