K-number	K791649
Device name	TETRAHYDROCANNALBINOL DIRECT BLOOD KIT
Applicant	Immunalysis Corporation
Product code	LAT
Device class	Class II
Decision date	Oct 11, 1979
Decision	Substantially Equivalent
Regulation	862.3870

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View the full FDA submission: accessdata.fda.gov

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TETRAHYDROCANNALBINOL DIRECT BLOOD KIT

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