K-number	K090455
Device name	PROVOX VEGA, MODEL 8130-8135
Applicant	Atos Medical AB
Product code	EWL
Device class	Class II
Decision date	Jun 5, 2009
Decision	Substantially Equivalent
Regulation	874.3730

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View the full FDA submission: accessdata.fda.gov

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PROVOX VEGA, MODEL 8130-8135

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