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

    THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP

    K Number: K955501 · Decision Jan 17, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    823
    Registration Numbers
    823
    Same Product Code
    2306
    Applicant Total
    24
    Review Days
    47

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    Basic Information

    Device Name
    THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP
    K Number
    K955501
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4400
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    The Tulip Mfg. Co.
    Date Received
    December 1, 1995
    Decision Date
    January 17, 1996
    Product Code
    GEI
    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
    GEI Electrosurgical, Cutting & Coagulation & Accessories

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    Other Clearances by The Tulip Mfg. Co.

    K Number Device Name
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    K955502 THE TULIP MONO POLAR ROTATABLE METZ SCISSORS
    K952901 THE TULIP COMPANY BRANSON #1 & #2 ELEVATOR
    K954734 THE TULIP LCI-200 ILLUMINATION & IMAGING SYSTEM (MODIFICATION)
    K952932 THE TULIP COMPANY BRANSON #1 ELEVATOR
    K952951 THE TULIP COMPANY BRASON NERVE HOOK & DISSECTOR
    K952953 THE TULIP CXOMPANY BRANSON #2 ELEVATOR
    K952902 THE TULIP COMPANY BRANSON POSTERIOR DISSECTOR
    K952958 THE TULIP COMPANY BRANSON OVERSHEATH
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