K-number	K043000
Device name	MODIFICATION TO D-TRONPLUS
Applicant	Disetronic Medical Systems AG
Product code	LZG
Device class	Class II
Decision date	Dec 1, 2004
Decision	Substantially Equivalent
Regulation	880.5725

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO D-TRONPLUS

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