ClearanceBrief
510(k) K993654 ยท HCC Device, Biofeedback

NEUROCOMP

ApplicantNeurocybernetics, Great Neck NY, US
DecisionSubstantially Equivalent, Jan 27, 2000
ReceivedOct 29, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K993654

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.