BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇧 United Kingdom

    LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001

    K Number: K031321 · Decision Jan 21, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    79
    Registration Numbers
    79
    Same Product Code
    221
    Applicant Total
    5
    Review Days
    271

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    Basic Information

    Device Name
    LIQUISHIELD LIQUID BANDAGE, MODEL LSB 0001
    K Number
    K031321
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.5090
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Medlogic Global Limited
    Date Received
    April 25, 2003
    Decision Date
    January 21, 2004
    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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