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

    BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B)

    K Number: K171404 · Decision Jul 17, 2017
    View on FDA
    Classifications
    1
    FEI Numbers
    34
    Registration Numbers
    34
    Same Product Code
    117
    Applicant Total
    4
    Review Days
    66

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    Basic Information

    Device Name
    BOSTON XO (hexafocon A), BOSTON XO2 (hexafocon B)
    K Number
    K171404
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.5916
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Bausch + Lomb, Incorporated
    Date Received
    May 12, 2017
    Decision Date
    July 17, 2017
    Product Code
    HQD
    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
    HQD Lens, Contact (Other Material) - Daily

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