BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

    ALLURA XPER FD SERIES / ALLURA XPER OR TABLE SERIES

    K Number: K141979 · Decision Aug 19, 2014
    View on FDA
    Classifications
    1
    FEI Numbers
    118
    Registration Numbers
    118
    Same Product Code
    319
    Applicant Total
    1
    Review Days
    29

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    Basic Information

    Device Name
    ALLURA XPER FD SERIES / ALLURA XPER OR TABLE SERIES
    K Number
    K141979
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    892.1650
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Philips Medical Systems Netherland BV
    Date Received
    July 21, 2014
    Decision Date
    August 19, 2014
    Product Code
    OWB
    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
    OWB Interventional Fluoroscopic X-Ray System

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