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

    ARAGON SURGICAL RF SYSTEM TELEO INSTRUMENT

    K Number: K093075 · Decision Jan 21, 2010
    View on FDA
    Classifications
    1
    FEI Numbers
    823
    Registration Numbers
    823
    Same Product Code
    2306
    Applicant Total
    6
    Review Days
    113

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    Basic Information

    Device Name
    ARAGON SURGICAL RF SYSTEM TELEO INSTRUMENT
    K Number
    K093075
    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
    Aragon Surgical, Inc.
    Date Received
    September 30, 2009
    Decision Date
    January 21, 2010
    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 Aragon Surgical, Inc.

    K Number Device Name
    K110824 ARAGON SURGICAL RF SYSTEM - 5MM LAPAROSCOPIC INSTRUMENT
    K090306 ARAGON SURGICAL RF SYSTEM L2 INSTRUMENT
    K081312 ARAGON ONESHOT SYSTEM
    K073452 MODIFICATION TO: ARAGON SURGICAL LAPCAP
    K070651 ARAGON SURGICAL LAPCAP