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510(k) Data Aggregation

    K Number
    K962837
    Device Name
    NULIFE
    Date Cleared
    1996-10-02

    (85 days)

    Product Code
    Regulation Number
    878.4460
    Why did this record match?
    Applicant Name (Manufacturer) :

    **MED-TECH RUBBER **& ENGINEERING INDUSTRIES

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K955055
    Device Name
    NULIFE
    Date Cleared
    1996-01-23

    (81 days)

    Product Code
    Regulation Number
    880.6250
    Why did this record match?
    Applicant Name (Manufacturer) :

    **MED-TECH RUBBER **& ENGINEERING INDUSTRIES

    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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