K-number	K772151
Device name	URINARY VMA - SCREEN TEST KIT
Applicant	Eppendorf-Brinkmann, Inc.
Product code	CDF
Device class	Class I
Decision date	Nov 30, 1977
Decision	Substantially Equivalent
Regulation	862.1795

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View the full FDA submission: accessdata.fda.gov

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URINARY VMA - SCREEN TEST KIT

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