ClearanceBrief
510(k) K760635 ยท FLS Monitor, Apnea, Facility Use

MEDI-DYNE APNEA MONITOR

ApplicantMed Dyne Inst., Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Sep 21, 1976
ReceivedSep 13, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K760635

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.