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

    AUTO. DEVEL. UNIT FOO DENTAL X-RAY

    K Number: K771433 · Decision Aug 19, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    8
    Applicant Total
    1
    Review Days
    18

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    Basic Information

    Device Name
    AUTO. DEVEL. UNIT FOO DENTAL X-RAY
    K Number
    K771433
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1900
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Ada Products Co., Inc.
    Date Received
    August 1, 1977
    Decision Date
    August 19, 1977
    Product Code
    EGY
    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
    EGY Processor, Radiographic-Film, Automatic, Dental

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