K-number	K042887
Device name	ACCU-CHEK SPIRIT
Applicant	Disetronic Medical Systems AG
Product code	LZG
Device class	Class II
Decision date	Mar 18, 2005
Decision	Substantially Equivalent
Regulation	880.5725

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Source

View the full FDA submission: accessdata.fda.gov

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ACCU-CHEK SPIRIT

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