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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 K222475
Device Name SNOR LOCK
Applicant
Solbaro Co., Ltd
4th fl. 137, Janggam-ro
Gamgok-myeon, Eumseong-gun,  KR 27603
Applicant Contact Donghoon Kim
Correspondent
Solbaro Co., Ltd
4th fl. 137, Janggam-ro
Gamgok-myeon, Eumseong-gun,  KR 27603
Correspondent Contact Jinwook Seo
Regulation Number872.5570
Classification Product Code
LRK  
Date Received08/16/2022
Decision Date 11/10/2022
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Dental
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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