K-number	K130856
Device name	BIA / VITALITY ANALYZER
Applicant	Ipgdx, LLC
Product code	MNW
Device class	Class II
Decision date	Nov 25, 2013
Decision	Substantially Equivalent
Regulation	870.2770

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Source

View the full FDA submission: accessdata.fda.gov

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BIA / VITALITY ANALYZER

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