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

    FITO DIDO

    K Number: K963075 · Decision Aug 22, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    1549
    Registration Numbers
    1550
    Same Product Code
    645
    Applicant Total
    2
    Review Days
    29

    Basic Information

    Device Name
    FITO DIDO
    K Number
    K963075
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    886.5850
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    FRAMESMART, INC.
    Date Received
    July 24, 1996
    Decision Date
    August 22, 1996
    Product Code
    HQY
    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
    HQY Sunglasses (Non-Prescription Including Photosensitive)

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