ClearanceBrief
510(k) K900560 ยท DQC Phonocardiograph

ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE

ApplicantAcuson Corp., Mountain View CA, US
DecisionSubstantially Equivalent, Dec 3, 1990
ReceivedFeb 7, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900560

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.