BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    EVERSTICK POST

    K Number: K030820 · Decision May 20, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    92
    Registration Numbers
    92
    Same Product Code
    34
    Applicant Total
    9
    Review Days
    67

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    Basic Information

    Device Name
    EVERSTICK POST
    K Number
    K030820
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.3810
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Stick Tech , Ltd.
    Date Received
    March 14, 2003
    Decision Date
    May 20, 2003
    Product Code
    ELR
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    ELR Post, Root Canal

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