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

    REINFORCING PIN

    K Number: K822412 · Decision Aug 30, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    51
    Registration Numbers
    51
    Same Product Code
    10
    Applicant Total
    1
    Review Days
    20

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    Basic Information

    Device Name
    REINFORCING PIN
    K Number
    K822412
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.3740
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Filhol
    Date Received
    August 10, 1982
    Decision Date
    August 30, 1982
    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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