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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 K120059
Device Name LIQUID BANDAGE
Applicant
Chesson Laboratory Associates, Inc.
603 Ellis Rd.
Durham,  NC  27703
Applicant Contact SCOTT E NEUVILLE
Correspondent
Chesson Laboratory Associates, Inc.
603 Ellis Rd.
Durham,  NC  27703
Correspondent Contact SCOTT E NEUVILLE
Regulation Number880.5090
Classification Product Code
KMF  
Date Received01/09/2012
Decision Date 05/17/2012
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
Predetermined Change
Control Plan Authorized		 No
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