ClearanceBrief
510(k) K862323 ยท HKI Camera, Ophthalmic, Ac-Powered

CANON NON-MYDRIATIC RETINAL CAMERA CR4-45NM

ApplicantCanon USA, Inc., Jericho NY, US
DecisionSubstantially Equivalent, Aug 21, 1986
ReceivedJun 19, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862323

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.