ClearanceBrief
510(k) K873599 ยท KQX Goniometer, Ac-Powered

EDI 320

ApplicantCybex, Ronkonkoma NY, US
DecisionSubstantially Equivalent, Oct 16, 1987
ReceivedSep 4, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K873599

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.