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

    IMAGE IV DICOM IMAGE ARCHIVAL PACS NETWORK

    K Number: K010058 · Decision Mar 21, 2001
    View on FDA
    Classifications
    1
    FEI Numbers
    609
    Registration Numbers
    609
    Same Product Code
    2221
    Applicant Total
    6
    Review Days
    72

    Basic Information

    Device Name
    IMAGE IV DICOM IMAGE ARCHIVAL PACS NETWORK
    K Number
    K010058
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.2050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    WITT BIOMEDICAL CORPORATION
    Date Received
    January 8, 2001
    Decision Date
    March 21, 2001
    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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