ClearanceBrief
510(k) K913079 ยท KQX Goniometer, Ac-Powered

02810-01/02810-02 ORTHORANGER II/02810-3 ROM 360

ApplicantLucas Sensing Systems, Inc., Phoenix AZ, US
DecisionSubstantially Equivalent, Sep 25, 1991
ReceivedJul 11, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K913079

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.