ClearanceBrief
510(k) K860361 ยท ITX Transducer, Ultrasonic, Diagnostic

DIASONICS 3.5 GWA 30MM PROBE

ApplicantDiasonics, Inc., Milipitas CA, US
DecisionSubstantially Equivalent, May 27, 1986
ReceivedJan 30, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860361

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.