ClearanceBrief
510(k) K963336 ยท DYG Catheter, Flow Directed

HARMAC THERMODILUTION CATHETER

ApplicantHarmac Medical Products, Inc., Buffalo NY, US
DecisionSubstantially Equivalent, Aug 14, 1997
ReceivedJun 28, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K963336

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.