ClearanceBrief
510(k) K834519 ยท HCC Device, Biofeedback

CALMTONE

ApplicantThought Technology , Ltd., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 30, 1984
ReceivedDec 21, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K834519

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.