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

    X-RAY TUBE - PANOBEAM

    K Number: K770345 · Decision Mar 8, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    9
    Registration Numbers
    9
    Same Product Code
    41
    Applicant Total
    1
    Review Days
    14

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    Basic Information

    Device Name
    X-RAY TUBE - PANOBEAM
    K Number
    K770345
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.1810
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Thoro-Ray, Inc.
    Date Received
    February 22, 1977
    Decision Date
    March 8, 1977
    Product Code
    EAP
    Advisory Committee
    Dental
    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
    EAP Unit, X-Ray, Intraoral

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