K-number	K051487
Device name	DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE
Applicant	Doctor'S Research Group, Inc.
Product code	KHJ
Device class	Class II
Decision date	Dec 22, 2005
Decision	Substantially Equivalent
Regulation	874.3620

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View the full FDA submission: accessdata.fda.gov

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DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE

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