ClearanceBrief
510(k) K992142 ยท DQO Catheter, Intravascular, Diagnostic

SCIMED ANGIOGRAPHIC CATHETERS

ApplicantScimed, Maple Grove MN, US
DecisionSubstantially Equivalent, Jul 21, 1999
ReceivedJun 24, 1999
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K992142

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.