BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    RITTER STARLIGHT DENTAL OPERATING LIGHT

    K Number: K760707 · Decision Oct 5, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    79
    Registration Numbers
    79
    Same Product Code
    22
    Applicant Total
    10
    Review Days
    12

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    Basic Information

    Device Name
    RITTER STARLIGHT DENTAL OPERATING LIGHT
    K Number
    K760707
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4630
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Ritter Co.
    Date Received
    September 23, 1976
    Decision Date
    October 5, 1976
    Product Code
    EAZ
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    EAZ Light, Operating, Dental

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