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

    NDS CORTISOL TEST KIT AND NDS CORTISOL CALIBRATOR

    K Number: K900010 · Decision Apr 3, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    13
    Registration Numbers
    13
    Same Product Code
    19
    Applicant Total
    58
    Review Days
    91

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    Basic Information

    Device Name
    NDS CORTISOL TEST KIT AND NDS CORTISOL CALIBRATOR
    K Number
    K900010
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1205
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Kallestad Diag, A Div. of Erbamont, Inc.
    Date Received
    January 2, 1990
    Decision Date
    April 3, 1990
    Product Code
    JFT
    Advisory Committee
    Clinical Chemistry
    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
    JFT Fluorometric, Cortisol

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