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510(k) Data Aggregation

    K Number
    K981949
    Device Name
    NUMOBAG
    Manufacturer
    Date Cleared
    1999-02-03

    (245 days)

    Product Code
    Regulation Number
    878.5650
    Why did this record match?
    Applicant Name (Manufacturer) :

    NUMOTECH, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    For adjunctive therapy of the following conditions: - Skin ulcerations due to diabetes, venous stasis, post surgical infections and gangrenous lesions - Decubitus ulcers - Amputations/infected stumps - Skin grafts - Burns - Frostbite
    Device Description
    Numobag™
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