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

    COHERENT FUNDUSL RETINAL CAMERA

    K Number: K822908 · Decision Jan 5, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    65
    Registration Numbers
    66
    Same Product Code
    155
    Applicant Total
    6
    Review Days
    97

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    Basic Information

    Device Name
    COHERENT FUNDUSL RETINAL CAMERA
    K Number
    K822908
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.1120
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    Coherent Medical Division
    Date Received
    September 30, 1982
    Decision Date
    January 5, 1983
    Product Code
    HKI
    Advisory Committee
    Ophthalmic
    Review Advisory Committee
    OP
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HKI Camera, Ophthalmic, Ac-Powered

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