K-number	K000247
Device name	BAUSCH & LOMB RENU 1 STEP DAILY PROTEIN REMOVER
Applicant	Bausch & Lomb, Inc.
Product code	LPN
Device class	Class II
Decision date	Apr 20, 2000
Decision	Substantially Equivalent
Regulation	886.5928

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View the full FDA submission: accessdata.fda.gov

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BAUSCH & LOMB RENU 1 STEP DAILY PROTEIN REMOVER

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