MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-03-09 for manufactured by .

MAUDE Entry Details


Device Details

Product CodeOAP
Date Received2017-03-09
Device AvailabilityI
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0



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