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510(k) Data Aggregation

    K Number
    K003010
    Device Name
    SPIRIT ACUPUNCTURE NEEDLE
    Manufacturer
    UNITED PACIFIC CO., LTD.
    Date Cleared
    2000-10-19

    (23 days)

    Product Code
    MQX
    Regulation Number
    880.5580
    Why did this record match?
    Applicant Name (Manufacturer) :

    UNITED PACIFIC CO., LTD.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
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    K Number
    K001718
    Device Name
    MILLENNIA ACUPUNCTURE NEEDLE
    Manufacturer
    UNITED PACIFIC CO., LTD.
    Date Cleared
    2000-06-21

    (16 days)

    Product Code
    MQX
    Regulation Number
    880.5580
    Why did this record match?
    Applicant Name (Manufacturer) :

    UNITED PACIFIC CO., LTD.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
    Ask a Question
    K Number
    K993123
    Device Name
    QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2B
    Manufacturer
    UNITED PACIFIC CO., LTD.
    Date Cleared
    1999-12-17

    (88 days)

    Product Code
    ILY
    Regulation Number
    890.5500
    Why did this record match?
    Applicant Name (Manufacturer) :

    UNITED PACIFIC CO., LTD.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Intented to use to emit energy in the infrared spectrum to provide topical heating for the purpose of temporarily elevating local tissue temperature. Intended to use for the temporary relief of minor muscle and joint stiffness, temporary relief of minor muscle strain spasm, temporary increase in local circulation where applied, and the relaxation of muscle.
    Device Description
    Not Found
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    K Number
    K991503
    Device Name
    SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36
    Manufacturer
    UNITED PACIFIC CO., LTD.
    Date Cleared
    1999-07-28

    (90 days)

    Product Code
    ILY
    Regulation Number
    890.5500
    Why did this record match?
    Applicant Name (Manufacturer) :

    UNITED PACIFIC CO., LTD.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    To emit energy in the infrared spectrum to provide topical temperature. Intended to use for the temporary relief of minor muscle and joint stiffness, temporary increase in local circulation where applied, and the relaxation of muscles.
    Device Description
    Not Found
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    K Number
    K990406
    Device Name
    KINGLI ACUPUNCTURE NEEDLE
    Manufacturer
    UNITED PACIFIC CO., LTD.
    Date Cleared
    1999-04-16

    (66 days)

    Product Code
    MQX, MOX
    Regulation Number
    880.5580
    Why did this record match?
    Applicant Name (Manufacturer) :

    UNITED PACIFIC CO., LTD.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    to pierce the skin in the practice of acupuncture by the states.
    Device Description
    DISPOSABLE ACUPUNCTURE NEEDLE
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