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

    THAYER MARTIN AGAR

    K Number: K811476 · Decision Jun 18, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    6
    Registration Numbers
    6
    Same Product Code
    82
    Applicant Total
    19
    Review Days
    23

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    Basic Information

    Device Name
    THAYER MARTIN AGAR
    K Number
    K811476
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.2410
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Biomedia, Inc.
    Date Received
    May 26, 1981
    Decision Date
    June 18, 1981
    Product Code
    JTY
    Advisory Committee
    Microbiology
    Review Advisory Committee
    TX
    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 Biomedia, Inc.

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    K821108 BI PLATE-XLD/HEKTOEN #30012
    K811478 EMB AGAR, LEVINE
    K811479 CHODOLATE AGAR, ENRICHED
    K811471 MUELLER HINTON AGAR
    K811475 TRYPTIC SOY AGAR W/5% & 10% SHEEP BLOOD
    K811473 MUELLER HINTON AGAR W/5% SHEEP BLOOD
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    Search all 19 clearances from Biomedia, Inc. →