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

    ENDOSCOPE AND ACCESSORIES

    K Number: K930082 · Decision Mar 15, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    1422
    Applicant Total
    4
    Review Days
    67

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    Basic Information

    Device Name
    ENDOSCOPE AND ACCESSORIES
    K Number
    K930082
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Weck Endoscopy
    Date Received
    January 7, 1993
    Decision Date
    March 15, 1993
    Product Code
    GCJ
    Advisory Committee
    Gastroenterology, Urology
    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
    GCJ Laparoscope, General & Plastic Surgery

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    Other Clearances by Weck Endoscopy

    K Number Device Name
    K926203 ENDOSCOPIC SCISSORS (DISPOSABLE/REUSABLE SHAFTS)
    K930550 ECO LIGATING CLIP
    K926223 ENDOSCOPE AND ACCESSORIES