K-number	K061804
Device name	ZERION ALPHA, ; ZERION BETA
Applicant	Etkon International GmbH
Product code	EIH
Device class	Class II
Decision date	Oct 6, 2006
Decision	Substantially Equivalent
Regulation	872.6660

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View the full FDA submission: accessdata.fda.gov

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ZERION ALPHA, ; ZERION BETA

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