K-number	K000963
Device name	DA VINCHI EEG AND EMG/EP SYSTEMS
Applicant	Airsep Corp.
Product code	GWF
Device class	Class II
Decision date	Oct 20, 2000
Decision	Substantially Equivalent
Regulation	882.1870

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View the full FDA submission: accessdata.fda.gov

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DA VINCHI EEG AND EMG/EP SYSTEMS

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