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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name device, jaw repositioning
510(k) Number K932932
Device Name SNOREMASTER SNORE REMEDY
Applicant
THE SNOREMASTER CO.
3530 HENRY AVE.
PHILADELPHIA,  PA  19129
Applicant Contact LEROY S FORNEY
Correspondent
THE SNOREMASTER CO.
3530 HENRY AVE.
PHILADELPHIA,  PA  19129
Correspondent Contact LEROY S FORNEY
Regulation Number872.5570
Classification Product Code
LQZ  
Date Received06/16/1993
Decision Date 02/10/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Type Traditional
Reviewed by Third Party No
Combination Product No
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