K-number	K921414
Device name	TROKEL /3 GONIO LASER LENS
Applicant	Ocular Instruments, Inc.
Product code	LQJ
Device class	Class II
Decision date	Nov 16, 1992
Decision	Substantially Equivalent
Regulation	886.4390

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View the full FDA submission: accessdata.fda.gov

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TROKEL /3 GONIO LASER LENS

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