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

    MODIFIED DPX BONE DENSITOMETER

    K Number: K890121 · Decision Apr 10, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    23
    Registration Numbers
    23
    Same Product Code
    146
    Applicant Total
    6
    Review Days
    454

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    Basic Information

    Device Name
    MODIFIED DPX BONE DENSITOMETER
    K Number
    K890121
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1170
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Lunar
    Date Received
    January 11, 1989
    Decision Date
    April 10, 1990
    Product Code
    KGI
    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
    KGI Densitometer, Bone

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    Other Clearances by Lunar

    K Number Device Name
    K914404 ORTHO SOFTWARE USED W/LUNAR DPX/DPX-L/DPS-@ DESIT
    K915535 FOREARM SOFTWARE FOR LUNAR DPX SERIES BONE DESITOM
    K905291 LATERAL SPINE DETERMAINATIONS DPX/DPX-L/DPX-ALPHA
    K904980 DPX-L AND DPX-ALPHA, MODIFICATION
    K884625 DPX BONE DENSITOMETER FOR TOTAL BODY BONE DENSITY