K-number	K082688
Device name	PRO HMPV+ ASSAY
Applicant	Prodesse, Inc.
Product code	OEM
Device class	Class II
Decision date	Nov 7, 2008
Decision	Substantially Equivalent
Regulation	866.3980

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View the full FDA submission: accessdata.fda.gov

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PRO HMPV+ ASSAY

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