K-number	K983172
Device name	ACCU-BASE HEMOGLOBIN A1C SAMPLE COLLECTION KIT
Applicant	Diabetes Technologies, Inc. (Dti)
Product code	LCP
Device class	Class II
Decision date	Nov 30, 1998
Decision	Substantially Equivalent
Regulation	864.7470

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Source

View the full FDA submission: accessdata.fda.gov

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ACCU-BASE HEMOGLOBIN A1C SAMPLE COLLECTION KIT

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