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

    SERIES 9000 LIFT-RECLINE CHAIR

    K Number: K903905 · Decision Sep 17, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    54
    Registration Numbers
    54
    Same Product Code
    52
    Applicant Total
    5
    Review Days
    25

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    Basic Information

    Device Name
    SERIES 9000 LIFT-RECLINE CHAIR
    K Number
    K903905
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    890.3110
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    Equi-Tron Mfg., Inc.
    Date Received
    August 23, 1990
    Decision Date
    September 17, 1990
    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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