ClearanceBrief
510(k) K946180 ยท DQX Wire, Guide, Catheter

SCIMED(R) ENTRE PTCA GUIDE WIRE

ApplicantScimed Life Systems, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Mar 17, 1995
ReceivedDec 20, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K946180

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.