K-number	K841831
Device name	CANNU-SKREEN-PRELIMINARY
Applicant	Biochemical Diagnostic, Inc.
Product code	DKE
Device class	Class II
Decision date	Jul 6, 1984
Decision	Substantially Equivalent
Regulation	862.3870

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View the full FDA submission: accessdata.fda.gov

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CANNU-SKREEN-PRELIMINARY

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