ClearanceBrief
510(k) K903562 ยท ITX Transducer, Ultrasonic, Diagnostic

CW DOPPLER 2.25 MHZ PROBE

ApplicantDiasonics, Inc., Milipitas CA, US
DecisionSubstantially Equivalent, Mar 2, 1992
ReceivedAug 7, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K903562

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.