K-number	K092364
Device name	MODEL 220 PATIENT MAGNET
Applicant	Cyberonics, Inc.
Product code	DTG
Device class	Class I
Decision date	Nov 3, 2009
Decision	Substantially Equivalent
Regulation	870.3690

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View the full FDA submission: accessdata.fda.gov

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MODEL 220 PATIENT MAGNET

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