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

    SITE PERISTALTIC MODULE SYSTEM

    K Number: K871375 · Decision May 7, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    36
    Registration Numbers
    36
    Same Product Code
    148
    Applicant Total
    30
    Review Days
    30

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    Basic Information

    Device Name
    SITE PERISTALTIC MODULE SYSTEM
    K Number
    K871375
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    886.4150
    Medical Specialty
    Ophthalmic
    Decision
    Substantially Equivalent
    Applicant
    Site Microsurgical Systems, Inc.
    Date Received
    April 7, 1987
    Decision Date
    May 7, 1987
    Product Code
    HQE
    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
    HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

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    Other Clearances by Site Microsurgical Systems, Inc.

    K Number Device Name
    K925828 MODIFIED SITE TXR SYSTEMS
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    K931866 SITE'S CD II PHACOEMULSIFICATION HANDPIECE
    K921135 IOLAB POWER I.V. POLE
    K920582 180 TIP, 1/A HANDPIECE .3MM END OPENING FOR OPHT.
    K912902 PHACOEMULSIFICATION SYSTEM FOR OPHTHALMIC USE
    K912739 SITE 90 TIP, I/A HANDPIECE .3MM SIDE OPEN/OPTH USE
    K910980 SITE 20 GAUGE REUSABLE FIBER OPTIC CABLE
    K905620 MODIFIED SITE PERISTALTIC FOOTSWITCH
    K904183 SITE PHACOEMULSIFICATION HANDPIECE
    Search all 30 clearances from Site Microsurgical Systems, Inc. →