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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 K102463
Device Name GOOD NIGHT
Applicant
LARRY V CONNELL, DMD
309 NORTH 84 AVE
YAKIMA,  WA  98908
Applicant Contact EILEEN CONNELL
Correspondent
LARRY V CONNELL, DMD
309 NORTH 84 AVE
YAKIMA,  WA  98908
Correspondent Contact EILEEN CONNELL
Regulation Number872.5570
Classification Product Code
LRK  
Date Received08/30/2010
Decision Date 05/25/2011
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Abbreviated
Reviewed by Third Party No
Combination Product No
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