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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 K923957
Device Name NASAL CAVITY WOUND DRESSING
Applicant
Smith & Nephew Richards, Inc.
2925 Appling Rd.
Bartlett,  TN  38133
Applicant Contact JEFF COBB
Correspondent
Smith & Nephew Richards, Inc.
2925 Appling Rd.
Bartlett,  TN  38133
Correspondent Contact JEFF COBB
Regulation Number880.5090
Classification Product Code
KMF  
Date Received08/06/1992
Decision Date 05/05/1993
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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