ClearanceBrief
510(k) K932218 ยท DQO Catheter, Intravascular, Diagnostic

CARDIAC CATH OR ANGIOGRAPHIC TRAYS

ApplicantAssociated Medical Products Co., St. Louis Park MN, US
DecisionUnknown, Aug 27, 1993
ReceivedMay 7, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K932218

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.