ClearanceBrief
510(k) K934359 ยท DQX Wire, Guide, Catheter

SCIMED STRIKE STEERABLE GUIDE WIRE

ApplicantScimed Peripheral Interventions, Plymouth MN, US
DecisionSubstantially Equivalent, Oct 7, 1993
ReceivedSep 8, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K934359

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.