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

    DIAGNOSTIC RADIOIMMUNOASSAY FOR QUANTI

    K Number: K822298 · Decision Sep 2, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    9
    Registration Numbers
    9
    Same Product Code
    44
    Applicant Total
    24
    Review Days
    30

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    Basic Information

    Device Name
    DIAGNOSTIC RADIOIMMUNOASSAY FOR QUANTI
    K Number
    K822298
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    862.1020
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Nuclear Medical Laboratories, Inc.
    Date Received
    August 3, 1982
    Decision Date
    September 2, 1982
    Product Code
    JFH
    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
    JFH Acid Phosphatase (Prostatic), Tartrate Inhibited

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