K-number	K003471
Device name	MAGNA TEK ESU-400
Applicant	Huttinger Medizintechnik GmbH & CO KG
Product code	GEI
Device class	Class II
Decision date	Nov 20, 2000
Decision	Substantially Equivalent
Regulation	—

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View the full FDA submission: accessdata.fda.gov

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MAGNA TEK ESU-400

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