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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 K002338
Device Name LIQUIDERM LIQUID ADHESIVE BANDAGE
Applicant
CLOSURE MEDICAL CORP.
5250 GREENS DAIRY RD.
RALEIGH,  NC  27616
Applicant Contact W. THOMAS STEPHENS
Correspondent
CLOSURE MEDICAL CORP.
5250 GREENS DAIRY RD.
RALEIGH,  NC  27616
Correspondent Contact W. THOMAS STEPHENS
Regulation Number880.5090
Classification Product Code
KMF  
Date Received08/01/2000
Decision Date 01/29/2001
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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