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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Fraction V, Antigen, Antiserum, Control
510(k) Number K822516
Device Name VIVONEX MASS GASTRASTOMY TUBE
Applicant
Norwich Eaton Pharmaceuticals, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Norwich Eaton Pharmaceuticals, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.5370
Classification Product Code
KHT  
Date Received08/20/1982
Decision Date 09/07/1982
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Immunology
510k Review Panel Immunology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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