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

    REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS

    K Number: K022748 · Decision Oct 9, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    153
    Registration Numbers
    153
    Same Product Code
    337
    Applicant Total
    5
    Review Days
    51

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    Basic Information

    Device Name
    REPROCSSED USED DISPOSABLE ENDOSCOPIC SCISSORS AND GRASPERS
    K Number
    K022748
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.1720
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Medical Device Services
    Date Received
    August 19, 2002
    Decision Date
    October 9, 2002
    Product Code
    HET
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HET Laparoscope, Gynecologic (And Accessories)

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    Other Clearances by Medical Device Services

    K Number Device Name
    K022753 REPROCESSES USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPS
    K022751 REPROCESSED USED DISPOSABLE HOT AND COLD BIOPSY FORCEPS
    K022743 REPROCESSED DISPOSABLE TROCARS
    K022744 REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS