K-number	K013194
Device name	UNIMARK HCG COMBO PREGNANCY TEST
Applicant	Biotech Atlantic, Inc.
Product code	JHI
Device class	Class II
Decision date	Oct 10, 2001
Decision	Substantially Equivalent
Regulation	862.1155

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View the full FDA submission: accessdata.fda.gov

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UNIMARK HCG COMBO PREGNANCY TEST

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