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

    A.C.S. SUTURE REMOVAL KIT

    K Number: K915827 · Decision Dec 8, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    56
    Registration Numbers
    56
    Same Product Code
    14
    Applicant Total
    1
    Review Days
    344

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    Basic Information

    Device Name
    A.C.S. SUTURE REMOVAL KIT
    K Number
    K915827
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Unknown
    Statement or Summary
    Statement
    Applicant
    American Carolina Stamping
    Date Received
    December 30, 1991
    Decision Date
    December 8, 1992
    Product Code
    MCZ
    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
    MCZ Suture Removal Kit

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