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

    VISITEC FLIERINGA-LEGRAND FIXATION RING

    K Number: K843195 · Decision Oct 5, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    12
    Registration Numbers
    12
    Same Product Code
    1
    Applicant Total
    49
    Review Days
    52

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    Basic Information

    Device Name
    VISITEC FLIERINGA-LEGRAND FIXATION RING
    K Number
    K843195
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    886.1750
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    Visitec Co.
    Date Received
    August 14, 1984
    Decision Date
    October 5, 1984
    Product Code
    HMH
    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
    HMH Rack, Skiascopic

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    SKIASCOPIC RACKS

    FDA 510(k)
    FDA Class 1 ·Ophthalmic
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