ClearanceBrief
510(k) K883597 ยท HCC Device, Biofeedback

MYODAC

ApplicantThought Technology , Ltd., Montreal, Quebec, CA
DecisionSubstantially Equivalent, Nov 16, 1988
ReceivedAug 22, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K883597

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.