K-number	K902136
Device name	KODAK SURECELL(TM) HCG-URINE TEST KIT
Applicant	Eastman Kodak Company
Product code	JHI
Device class	Class II
Decision date	Jun 28, 1990
Decision	Substantially Equivalent
Regulation	862.1155

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View the full FDA submission: accessdata.fda.gov

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KODAK SURECELL(TM) HCG-URINE TEST KIT

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