ClearanceBrief
510(k) K864812 ยท ITX Transducer, Ultrasonic, Diagnostic

DIASONICS SPA 3.5 MHZ, 30MM PROBE

ApplicantDiasonics, Inc., Milipitas CA, US
DecisionSubstantially Equivalent, Mar 10, 1987
ReceivedDec 9, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864812

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.