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

    POWERMAT VRP-1 X-RAY IMAGING

    K Number: K840698 · Decision Mar 16, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    52
    Registration Numbers
    52
    Same Product Code
    33
    Applicant Total
    1
    Review Days
    29

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    Basic Information

    Device Name
    POWERMAT VRP-1 X-RAY IMAGING
    K Number
    K840698
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    892.1840
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Powers Chemco, Inc.
    Date Received
    February 16, 1984
    Decision Date
    March 16, 1984
    Product Code
    IWZ
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    IWZ Film, Radiographic

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