ClearanceBrief
510(k) K893435 ยท DYG Catheter, Flow Directed

SILICONE FLOW-DIRECTED THERMODILUTION CATHETER

ApplicantCathlab Corp., Tustin CA, US
DecisionSubstantially Equivalent, Sep 26, 1989
ReceivedMay 2, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K893435

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.