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

    SYRETTE

    K Number: K881992 · Decision Jul 26, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    99
    Registration Numbers
    99
    Same Product Code
    71
    Applicant Total
    1
    Review Days
    75

    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
    SYRETTE
    K Number
    K881992
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4565
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Oratec Corp.
    Date Received
    May 12, 1988
    Decision Date
    July 26, 1988
    Product Code
    EKJ
    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
    EKJ Burnisher, Operative

    Similar 510(k) Clearances

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

    ASEPTYLUM, UNI-CARRIER

    FDA 510(k)
    FDA Class 1 ·Dental

    MEDTROL DENTAL KIT

    FDA 510(k)
    FDA Class 1 ·Dental

    DENTAL KIT

    FDA 510(k)
    FDA Class 1 ·Dental

    SUREFLEX FILES

    FDA 510(k)
    FDA Class 1 ·Dental

    INSTRUMENT,FILLING,PLASTIC,DENTAL

    FDA 510(k)
    FDA Class 1 ·Dental

    STAT PAK

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