K-number	K831051
Device name	HOME PREGNANCY TEST KIT HPK #1
Applicant	Quidel Corp.
Product code	LCX
Device class	Class II
Decision date	May 18, 1983
Decision	Substantially Equivalent
Regulation	862.1155

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View the full FDA submission: accessdata.fda.gov

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HOME PREGNANCY TEST KIT HPK #1

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