K-number	K931224
Device name	VIDAS TOTAL IGE (IGE) ASSAY
Applicant	Biomerieux Vitek, Inc.
Product code	DGP
Device class	Class II
Decision date	May 20, 1993
Decision	Substantially Equivalent
Regulation	866.5510

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View the full FDA submission: accessdata.fda.gov

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VIDAS TOTAL IGE (IGE) ASSAY

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