ClearanceBrief
510(k) K915554 ยท DQX Wire, Guide, Catheter

HI-TORQUE SPORT-T(TM) GUIDE WIRE

ApplicantPeripheral Systems Group, Mountain View CA, US
DecisionSubstantially Equivalent, Feb 9, 1993
ReceivedDec 11, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915554

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.