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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 K791815
Device Name MUELLER HINTON CHOCOLATE
Applicant
Isle Media and Sterile Products, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Isle Media and Sterile Products, Inc.
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.1700
Classification Product Code
JTZ  
Date Received09/14/1979
Decision Date 10/04/1979
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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