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

    PHILIPS INTEGRIS ALLURA FLAT DETECTOR RELEASE 1.0

    K Number: K022899 · Decision Nov 22, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    136
    Registration Numbers
    136
    Same Product Code
    299
    Applicant Total
    24
    Review Days
    80

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    Basic Information

    Device Name
    PHILIPS INTEGRIS ALLURA FLAT DETECTOR RELEASE 1.0
    K Number
    K022899
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1650
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Philips Medical Systems North America Co.
    Date Received
    September 3, 2002
    Decision Date
    November 22, 2002
    Product Code
    JAA
    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
    JAA System, X-Ray, Fluoroscopic, Image-Intensified

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