ClearanceBrief
510(k) K982770 ยท DQY Catheter, Percutaneous

6F ENVOY GUIDING CATHETER

ApplicantCordis Corp., Miami Lake FL, US
DecisionSubstantially Equivalent, Aug 18, 1998
ReceivedJul 23, 1998
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K982770

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.