ClearanceBrief
510(k) K915696 ยท ITX Transducer, Ultrasonic, Diagnostic

INTERSPEC APOGEE ENDO-V PROBE AND NEEDLE GUIDE

ApplicantInterspec, Inc., Ambler PA, US
DecisionSubstantially Equivalent, Nov 24, 1992
ReceivedDec 23, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K915696

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.