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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth
510(k) Number K842854
Device Name MUELLER HINTON BROTH
Applicant
Anarobe Systems
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Anarobe Systems
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.1700
Classification Product Code
JTZ  
Date Received07/20/1984
Decision Date 08/17/1984
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Microbiology
510k Review Panel Microbiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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