ClearanceBrief
510(k) K822991 ยท HKI Camera, Ophthalmic, Ac-Powered

AO DOCUSTAR(MMIRO) FUNDUS CAMERA

ApplicantWarner-Lambert Co., Walker MI, US
DecisionSubstantially Equivalent, Feb 24, 1983
ReceivedOct 12, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K822991

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.