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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 K926382
Device Name THERASNORE
Applicant
Dr. Thomas E. Meade
424 S. Washington St.
Alexandria,  VA  22314
Applicant Contact STEPHAN A BROWN
Correspondent
Dr. Thomas E. Meade
424 S. Washington St.
Alexandria,  VA  22314
Correspondent Contact STEPHAN A BROWN
Regulation Number872.5570
Classification Product Code
LRK  
Date Received12/22/1992
Decision Date 07/08/1993
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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