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

    VAC-RITE

    K Number: K770649 · Decision Jun 2, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    276
    Registration Numbers
    276
    Same Product Code
    47
    Applicant Total
    2
    Review Days
    57

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    Basic Information

    Device Name
    VAC-RITE
    K Number
    K770649
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6740
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Medical Development Co.
    Date Received
    April 6, 1977
    Decision Date
    June 2, 1977
    Product Code
    KDQ
    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
    KDQ Bottle, Collection, Vacuum

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