K-number	K872843
Device name	OVEIA (TM) DUAL ANALYTE
Applicant	Boots-Celltech Diagnostics, Inc.
Product code	JLP
Device class	Class I
Decision date	Feb 2, 1988
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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OVEIA (TM) DUAL ANALYTE

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