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

    MILLENNIA ACUPUNCTURE NEEDLE

    K Number: K001718 · Decision Jun 21, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    69
    Registration Numbers
    69
    Same Product Code
    90
    Applicant Total
    5
    Review Days
    16

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    Basic Information

    Device Name
    MILLENNIA ACUPUNCTURE NEEDLE
    K Number
    K001718
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5580
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    United Pacific Co., Ltd.
    Date Received
    June 5, 2000
    Decision Date
    June 21, 2000
    Product Code
    MQX
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    MQX Needle, Acupuncture, Single Use

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    Other Clearances by United Pacific Co., Ltd.

    K Number Device Name
    K003010 SPIRIT ACUPUNCTURE NEEDLE
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    K991503 SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36
    K990406 KINGLI ACUPUNCTURE NEEDLE