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

    SUTURE CUTTER

    K Number: K780574 · Decision Jul 17, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    251
    Registration Numbers
    251
    Same Product Code
    51
    Applicant Total
    2
    Review Days
    98

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    Basic Information

    Device Name
    SUTURE CUTTER
    K Number
    K780574
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Laschal Instrument Corp.
    Date Received
    April 10, 1978
    Decision Date
    July 17, 1978
    Product Code
    FZT
    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
    FZT Cutter, Surgical

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    SCISSORS, VARIOUS

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    Other Clearances by Laschal Instrument Corp.

    K Number Device Name
    K780575 LASCHAL SCISSOR