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

    BREVET DISPOSABLE CONNECTORS

    K Number: K895753 · Decision Nov 14, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    276
    Registration Numbers
    277
    Same Product Code
    889
    Applicant Total
    6
    Review Days
    49

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    Basic Information

    Device Name
    BREVET DISPOSABLE CONNECTORS
    K Number
    K895753
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1250
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Brevet, Inc.
    Date Received
    September 26, 1989
    Decision Date
    November 14, 1989
    Product Code
    DQY
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DQY Catheter, Percutaneous

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    Other Clearances by Brevet, Inc.

    K Number Device Name
    K910794 SMALL INSTRUMENT STERILIZATION/BUR BOX
    K895958 BREVET FLOSS PICK (AUTOCLAVE STERILIZER)
    K895959 BREVET FLOSS PICK (COLD STERILIZATION FLUIDS)
    K883126 BREVET DENTAL INSTRUMENTS
    K882617 BREVET CASSETTE STERILIZATION MODULE