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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Igm (Mu Chain Specific), Antigen, Antiserum, Control
510(k) Number K790705
Device Name ANTISERUM TO HUMAN IGM
Applicant
Kent Laboratories, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Kent Laboratories, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.5550
Classification Product Code
DAO  
Date Received04/12/1979
Decision Date 04/12/1979
Decision SE - Postmarket Surveillance Required (SESP)
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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