ClearanceBrief
510(k) K900155 ยท ITX Transducer, Ultrasonic, Diagnostic

INTERSPEC 2 MHZ, TRANSCRANIAL PULSED WAVE DOPPLER

ApplicantInterspec, Inc., Ambler PA, US
DecisionSubstantially Equivalent, Oct 5, 1990
ReceivedJan 12, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900155

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.