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

    WEE BAG O'MERCURY

    K Number: K840004 · Decision Mar 22, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    5
    Registration Numbers
    5
    Same Product Code
    5
    Applicant Total
    8
    Review Days
    78

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    Basic Information

    Device Name
    WEE BAG O'MERCURY
    K Number
    K840004
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.4610
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    Surgi-Quip Inc.U
    Date Received
    January 4, 1984
    Decision Date
    March 22, 1984
    Product Code
    LCC
    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
    LCC Applicator, Ocular Pressure

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    Other Clearances by Surgi-Quip Inc.U

    K Number Device Name
    K841115 CHARLES/MCINTYRE GIANT BREAK TABLE
    K841116 MOBILE OPHTHALMIC OPERATING TABLE
    K832887 ELECTRONIC UNIT
    K822427 SELF-CONTAINED MOBILE OPHTHAL. OPER. .
    K822554 CEMENT EXTRACTION INSTRUMENTATION
    K822426 MCINTYRE MICROSCOPE STAND
    K822428 SURGI-QUIP MICROSCOPE STAND