ClearanceBrief
510(k) K802183 ยท HKO Refractometer, Ophthalmic

SR-IV PROGRAMMED SUBJECTIVE REFRACTOR

ApplicantAmerican Optical Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 23, 1981
ReceivedSep 9, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K802183

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.