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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 K982893
Device Name 3M TEGASORB HYDROCOLLOID DRESSING
Applicant
3M Company
3m-Center
Bldg. 275-3e-08
St. Paul,  MN  55144
Applicant Contact ANNA E MCRIGHT
Correspondent
3M Company
3m-Center
Bldg. 275-3e-08
St. Paul,  MN  55144
Correspondent Contact ANNA E MCRIGHT
Regulation Number880.5090
Classification Product Code
KMF  
Date Received08/17/1998
Decision Date 10/26/1998
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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