ClearanceBrief
510(k) K941234 ยท HKI Camera, Ophthalmic, Ac-Powered

NON-MYDRIATIC RETINAL CAMERA

ApplicantCanon USA, Inc., Lake Success NY, US
DecisionSubstantially Equivalent, Jun 7, 1995
ReceivedMar 15, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K941234

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.