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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Staphylococcus Aureus Somatic Antigens
510(k) Number K812367
Device Name GOOSE BLOOD IN ALSEVER'S, CITRATED (ACD)
Applicant
Dutchland Laboratories, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Dutchland Laboratories, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.3700
Classification Product Code
LHT  
Date Received08/20/1981
Decision Date 09/09/1981
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Immunology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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