K-number	K072102
Device name	EPIVISION SL SYSTEM
Applicant	Gebauer Medizintechnik GmbH
Product code	HNO
Device class	Class I
Decision date	Jan 16, 2009
Decision	Substantially Equivalent
Regulation	886.4370

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View the full FDA submission: accessdata.fda.gov

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EPIVISION SL SYSTEM

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