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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 K062333
Device Name LAIMAD
Applicant
STEVEN LAMBERG, D.D.S
555 THIRTEEN STREET, NW
WASHINGTON,  DC  20004 -1109
Applicant Contact JONATHAN S KAHAN
Correspondent
STEVEN LAMBERG, D.D.S
555 THIRTEEN STREET, NW
WASHINGTON,  DC  20004 -1109
Correspondent Contact JONATHAN S KAHAN
Regulation Number872.5570
Classification Product Code
LRK  
Date Received08/10/2006
Decision Date 12/14/2006
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Abbreviated
Reviewed by Third Party No
Combination Product No
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