ClearanceBrief
510(k) K911073 ยท ITX Transducer, Ultrasonic, Diagnostic

PROBE REFILL KIT

ApplicantInterspec, Inc., Ambler PA, US
DecisionSubstantially Equivalent, Jun 6, 1991
ReceivedMar 11, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K911073

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.