ClearanceBrief
510(k) K923480 ยท DQO Catheter, Intravascular, Diagnostic

SCIMED ENTRE PTCA GUIDE WIRE AND RENDEZVOUS PTCA

ApplicantScimed Life Systems, Inc., Maple Grove MN, US
DecisionSubstantially Equivalent, Oct 6, 1992
ReceivedJul 15, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923480

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.