K-number	K050362
Device name	VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)
Applicant	Vident
Product code	EIH
Device class	Class II
Decision date	Mar 15, 2005
Decision	Substantially Equivalent
Regulation	872.6660

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View the full FDA submission: accessdata.fda.gov

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VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)

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