ClearanceBrief
510(k) K951567 ยท ITX Transducer, Ultrasonic, Diagnostic

CARDIOMETICS FLOWIRE, SMARTWIRE DOPPLER GUIDE WIRE

ApplicantCardio Metrics, Inc., Mountain View CA, US
DecisionSubstantially Equivalent, Oct 25, 1996
ReceivedApr 4, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951567

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.