K-number	K960438
Device name	TINTELIZE PAI-1 KIT
Applicant	Medical Diagnostic Technologies, Inc.
Product code	GGP
Device class	Class II
Decision date	Jun 5, 1996
Decision	Substantially Equivalent
Regulation	864.7290

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View the full FDA submission: accessdata.fda.gov

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TINTELIZE PAI-1 KIT

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