K-number	K974491
Device name	ACCU-CHEK A1C HEMOGLOBIN TEST
Applicant	Boehringer Mannheim Corp.
Product code	LCP
Device class	Class II
Decision date	May 13, 1998
Decision	Substantially Equivalent
Regulation	864.7470

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View the full FDA submission: accessdata.fda.gov

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ACCU-CHEK A1C HEMOGLOBIN TEST

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