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

    AUTOMASTER

    K Number: K904934 · Decision May 21, 1991
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    3
    Applicant Total
    3
    Review Days
    201

    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
    AUTOMASTER
    K Number
    K904934
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Team Mfg., Inc.
    Date Received
    November 1, 1990
    Decision Date
    May 21, 1991
    Product Code
    IPQ
    Advisory Committee
    Unknown
    Review Advisory Committee
    PM
    Third Party
    N

    Similar 510(k) Clearances

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

    SURE GRIP, HAND CONTROLS MODEL SG-1

    FDA 510(k)

    HAND CONTROLS, MODEL 3700 AND 3500 SERIES

    FDA 510(k)

    DADC '500' DRIVING CONTROL

    FDA 510(k)

    Other Clearances by Team Mfg., Inc.

    K Number Device Name
    K922055 STERILE AND NON-STERILE GAUZE SPONGES
    K922054 STERILE GAUZE SPONGES X-RAY DETECTABLE