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

    THAYER-MARTIN MEDIUM (MOD)

    K Number: K854275 · Decision Nov 12, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    6
    Registration Numbers
    6
    Same Product Code
    82
    Applicant Total
    12
    Review Days
    25

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    Basic Information

    Device Name
    THAYER-MARTIN MEDIUM (MOD)
    K Number
    K854275
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.2410
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    R. Kent Richards, Inc.
    Date Received
    October 18, 1985
    Decision Date
    November 12, 1985
    Product Code
    JTY
    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
    JTY Culture Media, For Isolation Of Pathogenic Neisseria

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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
    K854451 MUELLER HINTON MEDIUM
    Search all 12 clearances from R. Kent Richards, Inc. →