K-number	K090639
Device name	EXELO2, MODEL 4010
Applicant	Quantel Derma GmbH
Product code	ONG
Device class	Class II
Decision date	Oct 29, 2009
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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EXELO2, MODEL 4010

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