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510(k) Data Aggregation

    K Number
    K961316
    Device Name
    WOUND HYDROGEL AND/OR STERILE WOUND HYDROGEL
    Date Cleared
    1996-07-15

    (101 days)

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

    RENAISSANCE PHARMACEUTICAL, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K961766
    Device Name
    WOUND HYDROGEL & STERILE WOUND HYDROGEL
    Date Cleared
    1996-07-15

    (73 days)

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

    RENAISSANCE PHARMACEUTICAL, 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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