ClearanceBrief
510(k) K961280 ยท DQY Catheter, Percutaneous

SCIMED 6-10 F TRIGUIDE GUIDE CATHETERS 6F,7F,8F,9F & 10F

ApplicantScimed Life Systems, Inc., Maple Grove MN, US
DecisionSubstantially Equivalent, May 15, 1996
ReceivedApr 3, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K961280

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.