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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 K023163
Device Name LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020
Applicant
Medlogic Global Limited
Western Wood Way, Langage Science Park
Plympton, Plymouth, Devon,  GB PL7 5BG
Applicant Contact HOWARD BEAUMONT
Correspondent
Medlogic Global Limited
Western Wood Way, Langage Science Park
Plympton, Plymouth, Devon,  GB PL7 5BG
Correspondent Contact HOWARD BEAUMONT
Regulation Number880.5090
Classification Product Code
KMF  
Date Received09/23/2002
Decision Date 01/13/2003
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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