ClearanceBrief
510(k) K920678 ยท ITX Transducer, Ultrasonic, Diagnostic

ULTRASOUND IMAGAING SYSTEM AND DOPPLER FLOWMETER

ApplicantInterspec, Inc., Ambler PA, US
DecisionSubstantially Equivalent, Apr 2, 1992
ReceivedFeb 14, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920678

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.