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

    KIMAX QMA

    K Number: K022585 · Decision Oct 11, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    609
    Registration Numbers
    609
    Same Product Code
    2221
    Applicant Total
    3
    Review Days
    67

    Basic Information

    Device Name
    KIMAX QMA
    K Number
    K022585
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.2050
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    MEDICAL METRICS, INC.
    Date Received
    August 5, 2002
    Decision Date
    October 11, 2002
    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 MEDICAL METRICS, INC.

    K Number Device Name
    K013098 KIMAX REMOTE VIEWING STATION
    K010187 KIMAX, MODEL 1024