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

    KESTREL CONTACT LENS STORAGE CASE(POLYSTYRENE)

    K Number: K853729 · Decision Dec 13, 1985
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    73
    Applicant Total
    10
    Review Days
    98

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    Basic Information

    Device Name
    KESTREL CONTACT LENS STORAGE CASE(POLYSTYRENE)
    K Number
    K853729
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    Ryder Intl. Corp.
    Date Received
    September 6, 1985
    Decision Date
    December 13, 1985
    Product Code
    HPX
    Advisory Committee
    Unknown
    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
    HPX Lens, Contact (Polymethylmethacrylate)

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