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

    ADEL 5000

    K Number: K950889 · Decision Oct 16, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    6
    Applicant Total
    124
    Review Days
    230

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    Basic Information

    Device Name
    ADEL 5000
    K Number
    K950889
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.4900
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Stryker Corp.
    Date Received
    February 28, 1995
    Decision Date
    October 16, 1995
    Product Code
    HDD
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HDD Table, Obstetrical, Ac-Powered (And Accessories)

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