K-number	K130937
Device name	WAVE 2G, SOUL
Applicant	Hansaton Akustik GmbH
Product code	KLW
Device class	Class II
Decision date	Jan 3, 2014
Decision	Substantially Equivalent
Regulation	874.3400

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View the full FDA submission: accessdata.fda.gov

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WAVE 2G, SOUL

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