BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    PEREGRINE WET SET, MODEL PD400.00

    K Number: K990518 · Decision Mar 25, 1999
    View on FDA
    Classifications
    1
    FEI Numbers
    149
    Registration Numbers
    149
    Same Product Code
    847
    Applicant Total
    19
    Review Days
    35

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    Basic Information

    Device Name
    PEREGRINE WET SET, MODEL PD400.00
    K Number
    K990518
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5725
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Peregrine Surgical , Ltd.
    Date Received
    February 18, 1999
    Decision Date
    March 25, 1999
    Product Code
    FRN
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FRN Pump, Infusion

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