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

    NEUFINISH RESURFACING CREAM

    K Number: K982577 · Decision Oct 21, 1998
    View on FDA
    Classifications
    1
    FEI Numbers
    60
    Registration Numbers
    60
    Same Product Code
    146
    Applicant Total
    1
    Review Days
    89

    Basic Information

    Device Name
    NEUFINISH RESURFACING CREAM
    K Number
    K982577
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    NEUTROGENA CORP.
    Date Received
    July 24, 1998
    Decision Date
    October 21, 1998
    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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