ClearanceBrief
510(k) K123208 ยท HKI Camera, Ophthalmic, Ac-Powered

DIGITAL RETINAL CAMERA

ApplicantCanon Inc. -Medical Equipment Group, Bunkyo-Ku, Tokyo, JP
DecisionSubstantially Equivalent, Mar 19, 2013
ReceivedOct 12, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123208

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.