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

    MICROLINE FLEXIBLE LIGATING SHEARS

    K Number: K124029 · Decision Mar 27, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    823
    Registration Numbers
    823
    Same Product Code
    2306
    Applicant Total
    8
    Review Days
    89

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    Basic Information

    Device Name
    MICROLINE FLEXIBLE LIGATING SHEARS
    K Number
    K124029
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4400
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Microline Surgical, Inc.
    Date Received
    December 28, 2012
    Decision Date
    March 27, 2013
    Product Code
    GEI
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    GEI Electrosurgical, Cutting & Coagulation & Accessories

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    Other Clearances by Microline Surgical, Inc.

    K Number Device Name
    K234147 ReNew XR Handpiece, 25cm, with Reference Markings (3943M); ReNew XR Handpiece, 34cm, with Reference Markings (3941M); ReNew XR Handpiece, 42cm, with Reference Markings (3942M); ReNew XR Handpiece, Ratcheted, 25cm, with Reference Markings (3946M); ReNew XR Handpiece, Ratcheted, 34cm, with Reference Markings (3944M); ReNew XR Handpiece, Ratcheted, 42cm, with Reference Markings (3945M)
    K213127 ReNew Disposable Scissor Tips
    K201884 ReNew XR Handpiece, ReNew XR Handpiece 34cm, ReNew XR Handpiece 42cm, ReNew XR Handpiece 25cm, Ratcheted ReNew XR Handpiece 34cm
    K160706 ReNew V Handpiece Laparoscopic Instruments
    K152745 ReNew Sterilization Trays(Catalog #3708 and #3709)
    K152743 M/L-10 CLIP APPLIER STERILIZATION TRAY (Catalog#3706)
    K122086 THERMAL LIGATING SHEARS