ClearanceBrief
510(k) K940812 ยท KQX Goniometer, Ac-Powered

INSIGHT ELECTRONIC ALIGNMENT INDICATOR

ApplicantAndronic Devices, Ltd., Richmond, B.C. Canada V6v 2j2, CA
DecisionSubstantially Equivalent, Nov 21, 1994
ReceivedFeb 22, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940812

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.