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

    INTERP-1000

    K Number: K921476 · Decision Oct 21, 1992
    View on FDA
    Classifications
    0
    FEI Numbers
    11
    Registration Numbers
    11
    Same Product Code
    82
    Applicant Total
    11
    Review Days
    205

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    Basic Information

    Device Name
    INTERP-1000
    K Number
    K921476
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Qmed, Inc.
    Date Received
    March 30, 1992
    Decision Date
    October 21, 1992
    Product Code
    LOS
    Advisory Committee
    Unknown
    Review Advisory Committee
    CV
    Third Party
    N

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