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

    THE TULIP COMPANY BRASON NERVE HOOK & DISSECTOR

    K Number: K952951 · Decision Nov 14, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    548
    Registration Numbers
    548
    Same Product Code
    1422
    Applicant Total
    24
    Review Days
    141

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    Basic Information

    Device Name
    THE TULIP COMPANY BRASON NERVE HOOK & DISSECTOR
    K Number
    K952951
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    The Tulip Mfg. Co.
    Date Received
    June 26, 1995
    Decision Date
    November 14, 1995
    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 The Tulip Mfg. Co.

    K Number Device Name
    K952959 THE TULIP LAPAROSCOPE SHEATH 6MM DUAL STOPCOCK
    K952906 THE TULIP LAPAROSCOPE SHEATH 6MM SINGLE STOPCOCK
    K955502 THE TULIP MONO POLAR ROTATABLE METZ SCISSORS
    K955501 THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP
    K952901 THE TULIP COMPANY BRANSON #1 & #2 ELEVATOR
    K954734 THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM (MODIFICATION)
    K952932 THE TULIP COMPANY BRANSON #1 ELEVATOR
    K952953 THE TULIP CXOMPANY BRANSON #2 ELEVATOR
    K952902 THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR
    K952958 THE TULIP COMPANY BRANSON OVERSHEATH
    Search all 24 clearances from The Tulip Mfg. Co. →