BEUDAMED
    FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

    CILCO ANTERIOR CHAMBER LENS

    K Number: K771933 · Decision Jan 26, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    57
    Registration Numbers
    57
    Same Product Code
    4
    Applicant Total
    1
    Review Days
    104

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    Basic Information

    Device Name
    CILCO ANTERIOR CHAMBER LENS
    K Number
    K771933
    Device Class
    FDA class 3
    Clearance Type
    Traditional
    Regulation Number
    886.3600
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    California Intraocular Lens
    Date Received
    October 14, 1977
    Decision Date
    January 26, 1978
    Product Code
    HQL
    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
    HQL Intraocular Lens

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