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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Device, Anti-Snoring
510(k) Number K093710
Device Name THE MOSES APPLIANCE
Applicant
Allen J. Moses, Dds, Ltd.
233 S. Wacker Dr.
Chicago,  IL  60606
Applicant Contact ALLEN J MOSES
Correspondent
Allen J. Moses, Dds, Ltd.
233 S. Wacker Dr.
Chicago,  IL  60606
Correspondent Contact ALLEN J MOSES
Regulation Number872.5570
Classification Product Code
LRK  
Date Received12/02/2009
Decision Date 05/12/2010
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Statement Statement
Type Abbreviated
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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