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

    CONNECTOR 5 IN 1, T-CONNECTOR

    K Number: K830901 · Decision Apr 6, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    206
    Registration Numbers
    206
    Same Product Code
    26
    Applicant Total
    2
    Review Days
    16

    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
    CONNECTOR 5 IN 1, T-CONNECTOR
    K Number
    K830901
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6740
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Medical Specialists IN Packaging
    Date Received
    March 21, 1983
    Decision Date
    April 6, 1983
    Product Code
    GAZ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    GAZ Tubing, Noninvasive

    Similar 510(k) Clearances

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

    SUCTION/IRRIGATOR TUBING KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TUBING, NONINVASIVE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SUCTION/IRRIGATION Y TUBING SET W/TRUMPET VALVES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    NORTEC CONNECTING TUBE SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MEDID-VAC CLEAR NONCONDUCTIVE CONNECTING TUBE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MAXI-FLOW SUCTION SET W/Y CONNECTOR

    FDA 510(k)
    FDA Class 2 ·General Hospital
    View all

    Other Clearances by Medical Specialists IN Packaging

    K Number Device Name
    K831712 SURGICAL DRILL BITS