K-number	K002179
Device name	MAGNETOM ALLEGRA SYSTEM
Applicant	Siemens Medical Solutions USA, Inc.
Product code	LNH
Device class	Class II
Decision date	Oct 11, 2000
Decision	Substantially Equivalent
Regulation	892.1000

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View the full FDA submission: accessdata.fda.gov

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MAGNETOM ALLEGRA SYSTEM

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