ClearanceBrief
510(k) K946272 ยท DQY Catheter, Percutaneous

SCIMED(R) COURIER GUIDE CATHETER

ApplicantScimed Peripheral Interventions, Maple Grove MN, US
DecisionSubstantially Equivalent, Apr 17, 1995
ReceivedDec 23, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K946272

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.