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

    CAT-A-KIT

    K Number: K760920 · Decision Nov 9, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    1
    Applicant Total
    6
    Review Days
    12

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    Basic Information

    Device Name
    CAT-A-KIT
    K Number
    K760920
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.1165
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    The Upjohn Co.
    Date Received
    October 28, 1976
    Decision Date
    November 9, 1976
    Product Code
    CHT
    Advisory Committee
    Clinical Chemistry
    Review Advisory Committee
    CH
    Third Party
    N

    Classifications

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

    Product Code Device Name
    CHT Electrophoretic Method, Catecholamines

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