ClearanceBrief
510(k) K861064 ยท HLM Instrument, Measuring, Lens, Ac-Powered

LM-850 AUTOMATIC LENSMETER

ApplicantNidek, Inc., Palo Alto CA, US
DecisionSubstantially Equivalent, Apr 15, 1986
ReceivedMar 20, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K861064

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.