ClearanceBrief
510(k) K911439 ยท HKI Camera, Ophthalmic, Ac-Powered

NON-MYDRIATIC RETINAL CAMERA, CR-45UAF

ApplicantCanon USA, Inc., Tokyo 146, JP
DecisionSubstantially Equivalent, Jun 17, 1991
ReceivedApr 2, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K911439

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.