BEUDAMED
    FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

    STERILE WOUND HYDROGEL DRESSING

    K Number: K941339 · Decision Jun 10, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    51
    Registration Numbers
    51
    Same Product Code
    144
    Applicant Total
    4
    Review Days
    81

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    Basic Information

    Device Name
    STERILE WOUND HYDROGEL DRESSING
    K Number
    K941339
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Renaissance Pharmaceutical, Inc.
    Date Received
    March 21, 1994
    Decision Date
    June 10, 1994
    Product Code
    MGQ
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    MGQ Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic

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    Other Clearances by Renaissance Pharmaceutical, Inc.

    K Number Device Name
    K961316 WOUND HYDROGEL AND/OR STERILE WOUND HYDROGEL
    K961766 WOUND HYDROGEL & STERILE WOUND HYDROGEL
    K954384 WOUND HYDROGEL AND/OR STERILE WOUND HYDROGEL