K-number	K122237
Device name	BIOPHOTAS LIFELIGHT
Applicant	Biophotas, Inc.
Product code	ILY
Device class	Class II
Decision date	Jan 3, 2013
Decision	Substantially Equivalent
Regulation	890.5500

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Source

View the full FDA submission: accessdata.fda.gov

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BIOPHOTAS LIFELIGHT

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