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

    E.Z. LOCK WHEELCHAIR RESTRAINT DEVICE

    K Number: K894960 · Decision Sep 5, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    137
    Registration Numbers
    137
    Same Product Code
    63
    Applicant Total
    1
    Review Days
    29

    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
    E.Z. LOCK WHEELCHAIR RESTRAINT DEVICE
    K Number
    K894960
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.3920
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    E.Z. Lock, Inc.
    Date Received
    August 7, 1989
    Decision Date
    September 5, 1989
    Product Code
    KNN
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KNN Components, Wheelchair

    Similar 510(k) Clearances

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

    KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    DYNASTY GC 12550 (GELL/CELL)

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    DYNASTY GC 12400 (GELL/CELL)

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    DYNASTY U1-33 AGM

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    DYNASTY U1-31 (GELL/CELL)

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    ALDEN LINEAGE WHEELCHAIR CUSHION

    FDA 510(k)
    FDA Class 1 ·Physical Medicine
    View all