ClearanceBrief
510(k) K895010 ยท HLI Ophthalmoscope, Ac-Powered

MENTOR SPECTACLE BINOCULAR INDIRECT OPHTHALMOSCOPE

ApplicantMentor O & O, Inc., Norwell MA, US
DecisionSubstantially Equivalent, Sep 11, 1989
ReceivedAug 8, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895010

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.