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

    MUELLER HINTON MEDIUM

    K Number: K854451 · Decision Nov 18, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    73
    Applicant Total
    12
    Review Days
    13

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    Basic Information

    Device Name
    MUELLER HINTON MEDIUM
    K Number
    K854451
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.1700
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    R. Kent Richards, Inc.
    Date Received
    November 5, 1985
    Decision Date
    November 18, 1985
    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 R. Kent Richards, Inc.

    K Number Device Name
    K871065 CHLAMYDIA & VIRAL TRANSPORT MEDIUM
    K854452 MANNITOL SALT AGAR
    K854456 CAMPYLOBACTER BLOOD AGAR
    K854455 CDC ANAEROBE BLOOD AGAR
    K854454 TRYPTIC SOY BLOOD AGAR
    K854457 COLUMBIA CNA AGAR W/5% SHEEP BLOOD
    K854449 HEKTOEN ENTERIC AGAR
    K854453 P.E.Z. AGAR (PHENYLETHANOL AGAR)
    K854450 BILE ESCULIN AZIDE AGAR
    K854275 THAYER-MARTIN MEDIUM (MOD)
    Search all 12 clearances from R. Kent Richards, Inc. →