ClearanceBrief
510(k) K884188 ยท HLM Instrument, Measuring, Lens, Ac-Powered

NIDEK LM-870 AUTOMATIC LENSMETER

ApplicantNidek, Inc., Palo Alto CA, US
DecisionSubstantially Equivalent, Nov 23, 1988
ReceivedOct 5, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K884188

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.