ClearanceBrief
510(k) K925876 ยท HCG Device, Neurovascular Embolization

ITC BUNJI PLATINUM EMBOLIZATION COIL

ApplicantInterventional Therapeutics Corp., South San Francisco CA, US
DecisionSubstantially Equivalent, Apr 15, 1993
ReceivedNov 19, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925876

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.