K-number	K051209
Device name	LEVITRONIX CENTRIMAG BACK-UP CONSOLE
Applicant	Levitronix, LLC
Product code	KFM
Device class	Class II
Decision date	Sep 8, 2005
Decision	Substantially Equivalent
Regulation	870.4360

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Source

View the full FDA submission: accessdata.fda.gov

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LEVITRONIX CENTRIMAG BACK-UP CONSOLE

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