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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Antisera, Agglutinating, B. Pertussis, All
510(k) Number K781727
Device Name CHANGE IN STERILIZATION PROCEDURE
Applicant
Absorbent Cotton Co., Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Absorbent Cotton Co., Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.3065
Classification Product Code
GOY  
Date Received10/11/1978
Decision Date 12/04/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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