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

    IMPRUV A.I. CREAM WOUND AND SKIN EMULSION

    K Number: K041342 · Decision Jul 19, 2005
    View on FDA
    Classifications
    1
    FEI Numbers
    51
    Registration Numbers
    51
    Same Product Code
    144
    Applicant Total
    1
    Review Days
    425

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    Basic Information

    Device Name
    IMPRUV A.I. CREAM WOUND AND SKIN EMULSION
    K Number
    K041342
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Stiefel Laboratories, Inc.
    Date Received
    May 20, 2004
    Decision Date
    July 19, 2005
    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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