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

    E-VAC

    K Number: K073455 · Decision Mar 25, 2008
    View on FDA
    Classifications
    1
    FEI Numbers
    823
    Registration Numbers
    823
    Same Product Code
    2306
    Applicant Total
    2
    Review Days
    106

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    Basic Information

    Device Name
    E-VAC
    K Number
    K073455
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    878.4400
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    New Leaf Medical, Inc.
    Date Received
    December 10, 2007
    Decision Date
    March 25, 2008
    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 New Leaf Medical, Inc.

    K Number Device Name
    K061829 ELECTROSURGICAL CUTTING AND COAGULATION DEVICE AND ACCESSORIES