K-number	K833499
Device name	FIBERLAS 100 MEDICAL SYSTEM
Applicant	Fiberlase U.S.A.
Product code	LNK
Device class	Class II
Decision date	Apr 2, 1984
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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FIBERLAS 100 MEDICAL SYSTEM

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