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

    CERILLIUM

    K Number: K820049 · Decision Feb 22, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    94
    Registration Numbers
    94
    Same Product Code
    152
    Applicant Total
    2
    Review Days
    45

    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
    CERILLIUM
    K Number
    K820049
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3710
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Jelrus Technical Products Corp.
    Date Received
    January 8, 1982
    Decision Date
    February 22, 1982
    Product Code
    EJH
    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
    EJH Alloy, Metal, Base

    Similar 510(k) Clearances

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

    BEGOPAL+

    FDA 510(k)
    FDA Class 2 ·Dental

    CONTINUM V

    FDA 510(k)
    FDA Class 2 ·Dental

    CONTINUM

    FDA 510(k)
    FDA Class 2 ·Dental

    VERASOFT ES

    FDA 510(k)
    FDA Class 2 ·Dental

    DREAM BOND, DREAMCAST CHROME, DREAMCAST V, DREAM FLEXICAST, DREAM LITHECAST

    FDA 510(k)
    FDA Class 2 ·Dental

    WIROBOND C

    FDA 510(k)
    FDA Class 2 ·Dental
    View all

    Other Clearances by Jelrus Technical Products Corp.

    K Number Device Name
    K840254 DIAMOND LUSTRE