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

    ALLKARE(TM) ADHESIVE REMOVER WIPE

    K Number: K924976 · Decision Apr 20, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    102
    Registration Numbers
    102
    Same Product Code
    11
    Applicant Total
    81
    Review Days
    201

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    Basic Information

    Device Name
    ALLKARE(TM) ADHESIVE REMOVER WIPE
    K Number
    K924976
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4730
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Convatec, A Division of E.R. Squibb & Sons
    Date Received
    October 1, 1992
    Decision Date
    April 20, 1993
    Product Code
    KOX
    Advisory Committee
    General, Plastic Surgery
    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
    KOX Solvent, Adhesive Tape

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