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

    REGULATORS, LOW SUCTION

    K Number: K760316 · Decision Aug 4, 1976
    View on FDA
    Classifications
    1
    FEI Numbers
    29
    Registration Numbers
    29
    Same Product Code
    20
    Applicant Total
    7
    Review Days
    9

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    Basic Information

    Device Name
    REGULATORS, LOW SUCTION
    K Number
    K760316
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6740
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Harris-Lake, Inc.
    Date Received
    July 26, 1976
    Decision Date
    August 4, 1976
    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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