ClearanceBrief
510(k) K860568 ยท ITX Transducer, Ultrasonic, Diagnostic

ULTRASONIC IMAGING SYSTEM (MODIFIED)

ApplicantInterspec, Inc., Conshohocken PA, US
DecisionSubstantially Equivalent for Some Indications, Aug 11, 1986
ReceivedFeb 14, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860568

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.