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

    URIC ACID PROCEDURE, TEKPOINT DIRECT

    K Number: K770459 · Decision Apr 29, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    14
    Applicant Total
    30
    Review Days
    52

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    Basic Information

    Device Name
    URIC ACID PROCEDURE, TEKPOINT DIRECT
    K Number
    K770459
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    862.1775
    Medical Specialty
    Clinical Chemistry
    Decision
    Substantially Equivalent
    Applicant
    Icn Pharmaceuticals, Inc.
    Date Received
    March 8, 1977
    Decision Date
    April 29, 1977
    Product Code
    CDH
    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
    CDH Acid, Uric, Phosphotungstate Reduction

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