ClearanceBrief
510(k) K800768 ยท JAF Monitor, Ultrasonic, Nonfetal

VASCULAB BI-DIRECTIONAL DOPPLER, #D10

ApplicantMedasonics, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 8, 1980
ReceivedApr 7, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800768

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.