K-number	K030991
Device name	C. DIFF CHEK - 30
Applicant	Techlab, Inc.
Product code	LLH
Device class	Class I
Decision date	Jul 11, 2003
Decision	Substantially Equivalent
Regulation	866.2660

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View the full FDA submission: accessdata.fda.gov

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C. DIFF CHEK - 30

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