ClearanceBrief
510(k) K953579 ยท ITX Transducer, Ultrasonic, Diagnostic

TEE PROBE

ApplicantBiosound, Inc., Indianapolis IN, US
DecisionSubstantially Equivalent, Feb 2, 1996
ReceivedAug 1, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K953579

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.