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

    PARAGON MICRO-LOOPS

    K Number: K860022 · Decision Mar 24, 1986
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    80

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    Basic Information

    Device Name
    PARAGON MICRO-LOOPS
    K Number
    K860022
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Paragon Medical and Scientific, Inc.
    Date Received
    January 3, 1986
    Decision Date
    March 24, 1986
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N