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

    ROOT CANAL POST

    K Number: K924376 · Decision Nov 22, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    51
    Registration Numbers
    51
    Same Product Code
    10
    Applicant Total
    1
    Review Days
    451

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    Basic Information

    Device Name
    ROOT CANAL POST
    K Number
    K924376
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.3740
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    The Thera Group
    Date Received
    August 28, 1992
    Decision Date
    November 22, 1993
    Product Code
    EBL
    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
    EBL Pin, Retentive And Splinting, And Accessory Instruments

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