K-number	K010593
Device name	SUREVUE SERUM/URINE HCG, MODEL 1,30,50,100 TEST KIT
Applicant	Sa Scientific, Inc.
Product code	JHI
Device class	Class II
Decision date	Apr 5, 2001
Decision	Substantially Equivalent
Regulation	862.1155

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View the full FDA submission: accessdata.fda.gov

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SUREVUE SERUM/URINE HCG, MODEL 1,30,50,100 TEST KIT

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