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

    X-RAY CASSETTE

    K Number: K827379 · Decision May 19, 1982
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    30

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    X-RAY CASSETTE
    K Number
    K827379
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Synchroplan Corp.
    Date Received
    April 19, 1982
    Decision Date
    May 19, 1982
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N