BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    OCTAPETTES

    K Number: K823137 · Decision Dec 3, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    21
    Registration Numbers
    21
    Same Product Code
    65
    Applicant Total
    8
    Review Days
    39

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    Basic Information

    Device Name
    OCTAPETTES
    K Number
    K823137
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    866.2500
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Corning Costar Corp.
    Date Received
    October 25, 1982
    Decision Date
    December 3, 1982
    Product Code
    JTC
    Advisory Committee
    Microbiology
    Review Advisory Committee
    HE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JTC Device, Microtiter Diluting/Dispensing

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