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

    VTS-1000 VISUAL TESTING SYSTEM

    K Number: K812331 · Decision Nov 16, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    17
    Applicant Total
    26
    Review Days
    90

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    Basic Information

    Device Name
    VTS-1000 VISUAL TESTING SYSTEM
    K Number
    K812331
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.1630
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    Nicolet Biomedical Instruments
    Date Received
    August 18, 1981
    Decision Date
    November 16, 1981
    Product Code
    HLX
    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
    HLX Photostimulator, Ac-Powered

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