K-number	K834487
Device name	FLEXIBLE LIQUID LIGHT GUIDE
Applicant	Endo Lase, Inc.
Product code	FFS
Device class	Class II
Decision date	Feb 21, 1984
Decision	Substantially Equivalent
Regulation	876.1500

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View the full FDA submission: accessdata.fda.gov

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FLEXIBLE LIQUID LIGHT GUIDE

Everything you need for a 510(k) submission. Nothing you don't.