ClearanceBrief
510(k) K860553 ยท ITX Transducer, Ultrasonic, Diagnostic

STORZ, ALPHA II BIOMETRIC RULER

ApplicantStorz Instrument Co., St. Louis MO, US
DecisionSubstantially Equivalent, Jun 16, 1986
ReceivedFeb 14, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860553

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.