ClearanceBrief
510(k) K881984 ยท HLI Ophthalmoscope, Ac-Powered

EOL, MODEL LIO

ApplicantEol, Inc., Oak Ridge TN, US
DecisionSubstantially Equivalent, Sep 6, 1988
ReceivedMay 12, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K881984

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.