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

    VIRECTOMY LENS

    K Number: K940107 · Decision Sep 6, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    27
    Registration Numbers
    27
    Same Product Code
    40
    Applicant Total
    2
    Review Days
    239

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    Basic Information

    Device Name
    VIRECTOMY LENS
    K Number
    K940107
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.1385
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Visionary Technologies of Miami, Inc.
    Date Received
    January 10, 1994
    Decision Date
    September 6, 1994
    Product Code
    HJK
    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
    HJK Lens, Contact, Polymethylmethacrylate, Diagnostic

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    Other Clearances by Visionary Technologies of Miami, Inc.

    K Number Device Name
    K940106 KERATOPLASTY SUTURING LENS