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510(k) Data Aggregation

    K Number
    K961217
    Device Name
    BODILY FLUID DISPOSAL KIT
    Date Cleared
    1996-07-25

    (119 days)

    Product Code
    Regulation Number
    878.4040
    Why did this record match?
    Applicant Name (Manufacturer) :

    TRANSIDYNE GENERAL CORP.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K955658
    Device Name
    LACERATION TRAY
    Date Cleared
    1996-01-25

    (44 days)

    Product Code
    Regulation Number
    880.6850
    Why did this record match?
    Applicant Name (Manufacturer) :

    TRANSIDYNE GENERAL CORP.

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

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