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

    COXEL FLINGER 2500/5000 3-D IMAGING SYSTEM

    K Number: K912410 · Decision Aug 13, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    146
    Registration Numbers
    146
    Same Product Code
    1098
    Applicant Total
    2
    Review Days
    74

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    Basic Information

    Device Name
    COXEL FLINGER 2500/5000 3-D IMAGING SYSTEM
    K Number
    K912410
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1000
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Reality Imaging Corp.
    Date Received
    May 31, 1991
    Decision Date
    August 13, 1991
    Product Code
    LNH
    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
    LNH System, Nuclear Magnetic Resonance Imaging

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    Other Clearances by Reality Imaging Corp.

    K Number Device Name
    K883476 VOXEL FLINGER(TM) 3-D IMAGING SYSTEM