ClearanceBrief
510(k) K884611 ยท KQX Goniometer, Ac-Powered

THE ORTHORANGER II ELECTRONIC GONIOMETER

ApplicantMedical Instruments Technology, Inc., Alexandria VA, US
DecisionSubstantially Equivalent, Jan 31, 1989
ReceivedNov 4, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884611

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.