K-number	K953383
Device name	WYNTEK OSOM HCG-URINE TEST
Applicant	Wyntek Diagnostics, Inc.
Product code	JHI
Device class	Class II
Decision date	Aug 29, 1995
Decision	Substantially Equivalent
Regulation	862.1155

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View the full FDA submission: accessdata.fda.gov

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WYNTEK OSOM HCG-URINE TEST

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