ClearanceBrief
510(k) K980973 ยท DQO Catheter, Intravascular, Diagnostic

MEDTRONIC ANGIOGRAPHIC CATHETER

ApplicantMedtronics Interventional Vascular, Danvers MA, US
DecisionSubstantially Equivalent, Dec 10, 1998
ReceivedMar 16, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980973

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.