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

    DIGIRAD SYSTEM 1 AND THE REUSUABLE IMAGE MEDIA

    K Number: K852284 · Decision Nov 14, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    609
    Registration Numbers
    609
    Same Product Code
    2221
    Applicant Total
    3
    Review Days
    169

    Basic Information

    Device Name
    DIGIRAD SYSTEM 1 AND THE REUSUABLE IMAGE MEDIA
    K Number
    K852284
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.2050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    DIGI RAD CORP.
    Date Received
    May 29, 1985
    Decision Date
    November 14, 1985
    Product Code
    LLZ
    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
    LLZ System, Image Processing, Radiological

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    Other Clearances by DIGI RAD CORP.

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