ClearanceBrief
510(k) K925225 ยท KQX Goniometer, Ac-Powered

THE BTE VECTOR; ANALYSIS SYSTEM FOR THE LOW BACK

ApplicantBaltimore Therapeutic Equipment Co., Hanover MD, US
DecisionSubstantially Equivalent, Jun 27, 1994
ReceivedOct 16, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925225

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.