ClearanceBrief
510(k) K963663 ยท DQY Catheter, Percutaneous

11F GUIDING CATHETER

ApplicantBoston Scientific /International Technologies, San Diego CA, US
DecisionSubstantially Equivalent, Jan 13, 1997
ReceivedSep 13, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963663

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.