K-number	K012252
Device name	QUIK-CHECK OVULATION PREDICTOR
Applicant	ACON Laboratories, Inc.
Product code	CEP
Device class	Class I
Decision date	Aug 24, 2001
Decision	Substantially Equivalent
Regulation	862.1485

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Source

View the full FDA submission: accessdata.fda.gov

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QUIK-CHECK OVULATION PREDICTOR

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