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

    PILLING WECK SURGICAL Y STENT FORCEPS

    K Number: K990547 · Decision Apr 27, 1999
    View on FDA
    Classifications
    1
    FEI Numbers
    163
    Registration Numbers
    163
    Same Product Code
    238
    Applicant Total
    6
    Review Days
    64

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    Basic Information

    Device Name
    PILLING WECK SURGICAL Y STENT FORCEPS
    K Number
    K990547
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    874.4680
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Pilling Weck, Inc.
    Date Received
    February 22, 1999
    Decision Date
    April 27, 1999
    Product Code
    EOQ
    Advisory Committee
    Ear, Nose, Throat
    Review Advisory Committee
    EN
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    EOQ Bronchoscope (Flexible Or Rigid)

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    Other Clearances by Pilling Weck, Inc.

    K Number Device Name
    K974250 VERSASTAT MULTIPOLAR SCISSORS AND CABLES
    K962771 BURKE CONGENITAL THORACOSCOPY INSTRUMENTS
    K945520 HEMOCLIP ECOSYSTEM
    K944552 PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP
    K943719 VISISTAT STAPLER