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

    VA 1000

    K Number: K791380 · Decision Sep 19, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    9
    Applicant Total
    19
    Review Days
    57

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    Basic Information

    Device Name
    VA 1000
    K Number
    K791380
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.3720
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Vitatron Medical BV
    Date Received
    July 24, 1979
    Decision Date
    September 19, 1979
    Product Code
    DTA
    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
    DTA Tester, Pacemaker Electrode Function

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    K840668 ELECTRODE PACEMAKER, PERM & TEMP
    K831859 PACEMAKER PROGRAMMER #2032
    K831860 GENERATOR, PULSE, PACEMAKER #532
    K810928 ENDOCARDIAL ELECTRODE
    K791920 CARDIAC PACEMAKER P4000 SER. & P1000
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