ClearanceBrief
510(k) K854208 ยท HCC Device, Biofeedback

THE BODYLOG 500 RET THERAPEUTIC ELECTROMYOGRAPHICS

ApplicantBodylog, Inc., Mt. Kisco NY, US
DecisionSubstantially Equivalent, Jan 14, 1986
ReceivedOct 17, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854208

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.