ClearanceBrief
510(k) K132186 ยท HKI Camera, Ophthalmic, Ac-Powered

OPTOMED SMARTSCOPE M5 / OPTOMED SMARTSCOPE EY4 / OPTOMED SMARTSCOPE ES2

ApplicantOptomed OY, Oulu, FI
DecisionSubstantially Equivalent, Dec 18, 2013
ReceivedJul 15, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K132186

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.