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

    PROGESTERONE RADIOIMMUNOASSAY KIT

    K Number: K791051 · Decision Jul 24, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    47
    Registration Numbers
    47
    Same Product Code
    56
    Applicant Total
    9
    Review Days
    48

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    Basic Information

    Device Name
    PROGESTERONE RADIOIMMUNOASSAY KIT
    K Number
    K791051
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.1620
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Cis Radiopharmaceuticals, Inc.
    Date Received
    June 6, 1979
    Decision Date
    July 24, 1979
    Product Code
    JLS
    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
    JLS Radioimmunoassay, Progesterone

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