ClearanceBrief
510(k) K965023 ยท DQX Wire, Guide, Catheter

CHOICE PT PLUS PTCA GUIDE WIRE AND CHOICE PT VISION PTCA GUIDE WIRE

ApplicantScimed Life Systems, Inc., Maple Grove MN, US
DecisionSubstantially Equivalent, Mar 4, 1997
ReceivedDec 16, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K965023

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.