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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 K821428
Device Name MUELLER HINTON CHOCOLATE MED. ENRICHED
Applicant
Interstate Media
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Interstate Media
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number866.1700
Classification Product Code
JTZ  
Date Received05/12/1982
Decision Date 06/01/1982
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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