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

    MODIFIED PENOX LIFT CHAIR

    K Number: K862654 · Decision Jul 18, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    54
    Registration Numbers
    54
    Same Product Code
    52
    Applicant Total
    10
    Review Days
    7

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    Basic Information

    Device Name
    MODIFIED PENOX LIFT CHAIR
    K Number
    K862654
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.3110
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    Penox Technologies, Inc.
    Date Received
    July 11, 1986
    Decision Date
    July 18, 1986
    Product Code
    INO
    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
    INO Chair, Positioning, Electric

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    K851215 T-HANDLE ADAPTER, U-HANDLE & L HANDLER ADAPTER
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