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

    PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES

    K Number: K994151 · Decision Mar 1, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    321
    Registration Numbers
    322
    Same Product Code
    106
    Applicant Total
    9
    Review Days
    83

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    Basic Information

    Device Name
    PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICES
    K Number
    K994151
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Ximed/Prosure/Injectx
    Date Received
    December 9, 1999
    Decision Date
    March 1, 2000
    Product Code
    GAA
    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
    GAA Needle, Aspiration And Injection, Disposable

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    Other Clearances by Ximed/Prosure/Injectx

    K Number Device Name
    K002269 ELECTROSURGICAL PROBES AND DEVICES-GELTX
    K983765 INJECTION NEEDLE PROBE/DEVICE-TUNIS
    K983200 INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEX
    K981256 ISOLATED SALINE ELECTRODES/PROBES/DEVICES-SALINETRODE
    K974484 ISOLATED ELECTROSURGICAL PROBES AND DEVICES-SALINETRODE
    K974637 ELECTRODES/PROBES/DEVICES
    K962593 ELECTROSURGICAL PROBES & DEVICES
    K945995 BIPOLAR ELECTROSURGICAL PROBES AND INSTRUMENTS