ClearanceBrief
510(k) K902450 ยท HCC Device, Biofeedback

BODYLOG ENHANCED STRESS REDUCTION PACKAGE

ApplicantBodylog, Inc., Washington, D.C. DC, US
DecisionSubstantially Equivalent, Jan 25, 1991
ReceivedJun 1, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K902450

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.