K-number	K123031
Device name	BWF-5 MEDICAL LASER SERIES
Applicant	Litecure, LLC
Product code	GEX
Device class	Class II
Decision date	Dec 3, 2012
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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BWF-5 MEDICAL LASER SERIES

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