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

    MOVIT DEVICE

    K Number: K921710 · Decision Jun 29, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    58
    Registration Numbers
    58
    Same Product Code
    4
    Applicant Total
    1
    Review Days
    82

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    Basic Information

    Device Name
    MOVIT DEVICE
    K Number
    K921710
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.6100
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    John J. Navar, M.D.
    Date Received
    April 8, 1992
    Decision Date
    June 29, 1992
    Product Code
    BRY
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    BRY Cabinet, Table And Tray, Anesthesia

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