ClearanceBrief
510(k) K854277 ยท HCC Device, Biofeedback

NEUROPATH 4000

ApplicantTherapeutic Technologies, Inc., Washington DC, US
DecisionSubstantially Equivalent, Jan 21, 1986
ReceivedOct 23, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K854277

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.