K-number	K852798
Device name	FIBERLASE 100 MEDICAL LASER SYSTEM
Applicant	Laser Media
Product code	LNK
Device class	Class II
Decision date	Jul 29, 1985
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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FIBERLASE 100 MEDICAL LASER SYSTEM

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