K-number	K974615
Device name	QUICKSTICK PRO HCG TEST
Applicant	Phamatech
Product code	JHI
Device class	Class II
Decision date	Jan 26, 1998
Decision	Substantially Equivalent
Regulation	862.1155

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View the full FDA submission: accessdata.fda.gov

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QUICKSTICK PRO HCG TEST

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