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

    HOWMEDICA BRASS CENTER DISC

    K Number: K790640 · Decision May 1, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    90
    Registration Numbers
    90
    Same Product Code
    3
    Applicant Total
    1
    Review Days
    32

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    HOWMEDICA BRASS CENTER DISC
    K Number
    K790640
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.6010
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    E.C. Moore Co.
    Date Received
    March 30, 1979
    Decision Date
    May 1, 1979
    Product Code
    EHJ
    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
    EHJ Disk, Abrasive

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (EHJ), ordered by most recent decision date.

    MICROMILLS, PATRIOTS, ALPHA GOLD DIAMONDS

    FDA 510(k)
    FDA Class 1 ·Dental

    MIN-IDENTOFLEX

    FDA 510(k)
    FDA Class 1 ·Dental

    IDENTOFLEX

    FDA 510(k)
    FDA Class 1 ·Dental
    View all