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

    AUTOMATIC EXPOSURE CONTROL TYPE A3300

    K Number: K827525 · Decision Jun 18, 1982
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    5
    Review Days
    28

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    Basic Information

    Device Name
    AUTOMATIC EXPOSURE CONTROL TYPE A3300
    K Number
    K827525
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Advanced Instrument Development, Inc.
    Date Received
    May 21, 1982
    Decision Date
    June 18, 1982
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

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