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510(k) Data Aggregation

    K Number
    K011248
    Device Name
    CW DISPOSABLE ACUPUNCTURE NEEDLE
    Manufacturer
    ACUSUPPLY, INC.
    Date Cleared
    2001-10-29

    (189 days)

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

    ACUSUPPLY, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K011247
    Device Name
    HOLY DRAGON STERILE ACUPUNCTURE NEEDLE FOR SINGLE USE
    Manufacturer
    ACUSUPPLY, INC.
    Date Cleared
    2001-10-17

    (177 days)

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

    ACUSUPPLY, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
    Ask a Question

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    K Number
    K011242
    Device Name
    HUANQIU AND SUPER (TWO BRANDS) STERILE ACUPUNCTURE NEEDLE FOR SINGLE USE
    Manufacturer
    ACUSUPPLY, INC.
    Date Cleared
    2001-09-11

    (141 days)

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

    ACUSUPPLY, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
    Ask a Question

    Ask a specific question about this device

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