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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name bandage, liquid
510(k) Number K083913
Device Name CHESSON LABS LIQUID BANDAGE
Applicant
CHESSON LABORATORY ASSOCIATES, INC.
3100 TOWER BLVD., SUITE 117
DURHAM,  NC  27707
Applicant Contact SCOTT E NEUVILLE
Correspondent
CHESSON LABORATORY ASSOCIATES, INC.
3100 TOWER BLVD., SUITE 117
DURHAM,  NC  27707
Correspondent Contact SCOTT E NEUVILLE
Regulation Number880.5090
Classification Product Code
KMF  
Date Received12/30/2008
Decision Date 07/31/2009
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
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