BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP

    K Number: K944552 · Decision Nov 7, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    112
    Registration Numbers
    112
    Same Product Code
    175
    Applicant Total
    6
    Review Days
    52

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    Basic Information

    Device Name
    PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP
    K Number
    K944552
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4300
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Pilling Weck, Inc.
    Date Received
    September 16, 1994
    Decision Date
    November 7, 1994
    Product Code
    FZP
    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
    FZP Clip, Implantable

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    Other Clearances by Pilling Weck, Inc.

    K Number Device Name
    K990547 PILLING WECK SURGICAL Y STENT FORCEPS
    K974250 VERSASTAT MULTIPOLAR SCISSORS AND CABLES
    K962771 BURKE CONGENITAL THORACOSCOPY INSTRUMENTS
    K945520 HEMOCLIP ECOSYSTEM
    K943719 VISISTAT STAPLER