ClearanceBrief
510(k) K133758 ยท HLI Ophthalmoscope, Ac-Powered

CENTERVUE MACULAR INTEGRITY ASSESSMENT

ApplicantCentervue S.P.A., Rome, IT
DecisionSubstantially Equivalent, Apr 23, 2014
ReceivedDec 11, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K133758

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.