K-number	K853539
Device name	ABBOTT TESTPACK HCG(URINE) DIAGNOSTIC KIT
Applicant	Abbott Laboratories
Product code	JHI
Device class	Class II
Decision date	Sep 25, 1985
Decision	Substantially Equivalent
Regulation	862.1155

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View the full FDA submission: accessdata.fda.gov

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ABBOTT TESTPACK HCG(URINE) DIAGNOSTIC KIT

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