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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Gauze / Sponge,Nonresorbable For External Use
510(k) Number K791166
Device Name DEXIDE DISPOSABLE PREP SPONGE
Applicant
Dexide, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Dexide, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number878.4014
Classification Product Code
NAB  
Date Received06/25/1979
Decision Date 07/10/1979
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
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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