K-number	K861064
Device name	LM-850 AUTOMATIC LENSMETER
Applicant	Nidek, Inc.
Product code	HLM
Device class	Class I
Decision date	Apr 15, 1986
Decision	Substantially Equivalent
Regulation	886.1425

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View the full FDA submission: accessdata.fda.gov

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LM-850 AUTOMATIC LENSMETER

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