ClearanceBrief
510(k) K800655 ยท DQC Phonocardiograph

MODEL 100 SPECTRAVIEW

ApplicantEdwards Laboratories, Mchenry IL, US
DecisionSubstantially Equivalent, Apr 16, 1980
ReceivedMar 25, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800655

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.