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

    AOI LC-40 PHACOEMULSIFIER

    K Number: K952331 · Decision Aug 16, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    73
    Registration Numbers
    73
    Same Product Code
    315
    Applicant Total
    6
    Review Days
    90

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    Basic Information

    Device Name
    AOI LC-40 PHACOEMULSIFIER
    K Number
    K952331
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.4670
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    American Optisurgical, Inc.
    Date Received
    May 18, 1995
    Decision Date
    August 16, 1995
    Product Code
    HQC
    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
    HQC Unit, Phacofragmentation

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    Other Clearances by American Optisurgical, Inc.

    K Number Device Name
    K101561 TX1 TISSUE REMOVAL SYSTEM
    K080803 VISUAL PHACOEMULSIFICATION SYSTEM, MODEL 551
    K020527 HORIZON PHACOEMULSIFICATION SYSTEM, MODEL HZN-2030
    K953538 RM001 REUSABLE
    K953539 DM001 DISPOSABLE PACK