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

    VACUUM REGULATOR 0-2000 MMHG VR-1000

    K Number: K834224 · Decision Feb 27, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    29
    Registration Numbers
    29
    Same Product Code
    20
    Applicant Total
    1
    Review Days
    83

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    Basic Information

    Device Name
    VACUUM REGULATOR 0-2000 MMHG VR-1000
    K Number
    K834224
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6740
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Trimeter Instrument Corp.
    Date Received
    December 6, 1983
    Decision Date
    February 27, 1984
    Product Code
    KDP
    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
    KDP Regulator, Vacuum

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