ClearanceBrief
510(k) K915347 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

SCIMED VIPER CATHETER

ApplicantScimed, Maple Grove MN, US
DecisionSubstantially Equivalent, Aug 17, 1992
ReceivedNov 26, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915347

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.