6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MAX-ACT
FDA 510(k)
FDA Class 2
·Hematology
Diagnostic Fixed Electrophysiology Catheter, Diagnostic Electrophysiology Cable
FDA 510(k)
FDA Class 2
·Cardiovascular
CARDIUS 3 X-ACT
FDA 510(k)
FDA Class 2
·Radiology
SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·February 28, 2013
VOYAGER RX CORONARY DILATATION CATHETER
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code LOX·February 10, 2011
PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)
FDA Adverse Event
Malfunction
·INVACARE FLORIDA OPERATIONS·Product code CAW·August 6, 2014