BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    MUELLER HINTON MEDIUM

    K Number: K821430 · Decision Jun 1, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    73
    Applicant Total
    15
    Review Days
    20

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    Basic Information

    Device Name
    MUELLER HINTON MEDIUM
    K Number
    K821430
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.1700
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Interstate Media
    Date Received
    May 12, 1982
    Decision Date
    June 1, 1982
    Product Code
    JTZ
    Advisory Committee
    Microbiology
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    JTZ Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/Broth

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    Other Clearances by Interstate Media

    K Number Device Name
    K821422 SS AGAR
    K821417 TRYPTIC SOY AGAR W/10% SHEEP BLOOD
    K821418 TRYPTOSE BLOOD AGAR W/5% SHEEP BLOOD
    K821425 COLUMBIA BLOOD AGAR W/5% SHEEP BLOOD
    K821419 EMB AGAR
    K821428 MUELLER HINTON CHOCOLATE MED. ENRICHED
    K821426 STAPHYLOCOCCUS MEDIUM 1100
    K821420 EMB AGAR
    K821429 MUELLER HINTON MED. W/5% SHEEP BLOOD
    K821427 MANNITOL SALT AGAR
    Search all 15 clearances from Interstate Media →