ClearanceBrief
510(k) K810332 ยท HCC Device, Biofeedback

SC/TEMP 300

ApplicantThought Technology , Ltd., Mchenry IL, US
DecisionSubstantially Equivalent, May 18, 1981
ReceivedFeb 9, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810332

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.