BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    NASP HYDROCOLLOID DRESSING (REGULAR OR THIN)

    K Number: K964231 · Decision Mar 10, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    79
    Registration Numbers
    79
    Same Product Code
    221
    Applicant Total
    16
    Review Days
    138

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    Basic Information

    Device Name
    NASP HYDROCOLLOID DRESSING (REGULAR OR THIN)
    K Number
    K964231
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.5090
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    North American Sterilization & Packaging Co.
    Date Received
    October 23, 1996
    Decision Date
    March 10, 1997
    Product Code
    KMF
    Advisory Committee
    General Hospital
    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
    KMF Bandage, Liquid

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