K-number	K101771
Device name	RELINE-IT MODEL RELINE-IT
Applicant	Majestic Drug Co., Inc.
Product code	EBP
Device class	Class II
Decision date	Sep 20, 2010
Decision	Substantially Equivalent
Regulation	872.3560

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View the full FDA submission: accessdata.fda.gov

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RELINE-IT MODEL RELINE-IT

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