BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

    CDR SYSTEMS PRECISION PATIENT POSITIONING SYSTEM

    K Number: K122888 · Decision Apr 30, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    114
    Registration Numbers
    114
    Same Product Code
    733
    Applicant Total
    1
    Review Days
    222

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    Basic Information

    Device Name
    CDR SYSTEMS PRECISION PATIENT POSITIONING SYSTEM
    K Number
    K122888
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.5050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Cdr Systems, Inc.
    Date Received
    September 20, 2012
    Decision Date
    April 30, 2013
    Product Code
    IYE
    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
    IYE Accelerator, Linear, Medical

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