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

    INSTATEMP

    K Number: K770944 · Decision Jul 27, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    29
    Registration Numbers
    29
    Same Product Code
    20
    Applicant Total
    1
    Review Days
    63

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    Basic Information

    Device Name
    INSTATEMP
    K Number
    K770944
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.6740
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    H.I. Silverman, D.Sc.
    Date Received
    May 25, 1977
    Decision Date
    July 27, 1977
    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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