K-number	K870197
Device name	KDI QUIK TEST(TM) MARIJUANA SCREEN
Applicant	Keystone Diagnostics, Inc.
Product code	LDJ
Device class	Class II
Decision date	Jun 1, 1987
Decision	Substantially Equivalent
Regulation	862.3870

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View the full FDA submission: accessdata.fda.gov

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KDI QUIK TEST(TM) MARIJUANA SCREEN

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