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

    RETREAT

    K Number: K801606 · Decision Jul 28, 1980
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    13

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    Basic Information

    Device Name
    RETREAT
    K Number
    K801606
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Omnitronics Research Corp.
    Date Received
    July 15, 1980
    Decision Date
    July 28, 1980
    Advisory Committee
    Unknown
    Review Advisory Committee
    NE
    Third Party
    N