ClearanceBrief
510(k) K900386 ยท DQX Wire, Guide, Catheter

ACS ADVANCED CONCEPT GUIDE WIRE

ApplicantAdvanced Cardiovascular Systems, Inc., Santa Clara CA, US
DecisionSubstantially Equivalent, Jun 12, 1990
ReceivedJan 29, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900386

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.