ClearanceBrief
510(k) K923708 ยท HKI Camera, Ophthalmic, Ac-Powered

LEMPERT OPTIC DISC ANALYSIS SYSTEM

ApplicantLempert Ophthalmic Instruments, Ithaca NY, US
DecisionSubstantially Equivalent, Mar 19, 1993
ReceivedJul 27, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923708

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.