ClearanceBrief
510(k) K861065 ยท HKO Refractometer, Ophthalmic

AR-1100 AUTOMATIC REFRACTOR

ApplicantNidek, Inc., Palo Alto CA, US
DecisionSubstantially Equivalent, Apr 9, 1986
ReceivedMar 20, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K861065

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.