ClearanceBrief
510(k) K864943 ยท DQO Catheter, Intravascular, Diagnostic

NUMED BALLOON WEDGE PRESSURE CATHETER

ApplicantNuMED, Inc., Hopkinton NY, US
DecisionSubstantially Equivalent, Feb 20, 1987
ReceivedDec 17, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864943

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.