K-number	K210103
Device name	SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX
Applicant	Lifelong Meditech Private Limited
Product code	FMF
Device class	Class II
Decision date	Jul 16, 2021
Decision	Substantially Equivalent
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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SAFEWAY, LIFELONG PREMIUM, LIFELONG MATRIX

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