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

    MINIBORE STOPCOCK SET

    K Number: K954984 · Decision Jan 23, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    88
    Registration Numbers
    88
    Same Product Code
    88
    Applicant Total
    8
    Review Days
    84

    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
    MINIBORE STOPCOCK SET
    K Number
    K954984
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Distronic Sterile Products, Inc.
    Date Received
    October 31, 1995
    Decision Date
    January 23, 1996
    Product Code
    FMG
    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
    FMG Stopcock, I.V. Set

    Similar 510(k) Clearances

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

    Qitexio® 4-Way Stopcock (QIT014)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Three Way Stop Cock

    FDA 510(k)
    FDA Class 2 ·General Hospital

    lntravascular Administration Sets with Stopcock and Manifold

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SafePort(TM) Manifold (or Stopcock)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Clicky Cross

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TurnSignal Stopcocks Sterile, TurnSignal Stopcocks Buld Non Sterile, TurnSignal Stopcocks with Manifolds Sterile, TurnSignal Stopcocks with Manifolds Bulk Non Sterile

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

    Other Clearances by Distronic Sterile Products, Inc.

    K Number Device Name
    K955732 VENTED SOLUTION SET
    K955709 WINGED & SUBCUTANEOUS INFUSION SETS
    K954983 EXTENSION SET WITH CHECK VALVE
    K952664 SOLUTION ADMINISTRATION SET
    K950597 CORE-RESISTANT HUBER INFUSION SET WITH Y-SITE
    K952663 60 MICRO VOLUME EXTENSION SET W/.22 MICRON FILTER, 21 EXTENSION SET W/1.2 MIVTON GILYRT, INJ. SITE, CLAMP
    K945184 INTRAVASCULAR ADMINISTRATION SET