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

    TOCO LITE, MODEL TD-01

    K Number: K013477 · Decision Jan 17, 2002
    View on FDA
    Classifications
    1
    FEI Numbers
    15
    Registration Numbers
    15
    Same Product Code
    22
    Applicant Total
    5
    Review Days
    90

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    Basic Information

    Device Name
    TOCO LITE, MODEL TD-01
    K Number
    K013477
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.2720
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Ventrex, Inc.
    Date Received
    October 19, 2001
    Decision Date
    January 17, 2002
    Product Code
    HFM
    Advisory Committee
    Obstetrics/Gynecology
    Review Advisory Committee
    OB
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    HFM Monitor, Uterine Contraction, External (For Use In Clinic)

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    Other Clearances by Ventrex, Inc.

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    K061044 FEATHERLITE AQUA TOCODYNAMOMETER
    K964821 COVEROX SHEATH MODELS NUMBER PS65, PS67, EPS65 AND EPS67
    K925044 VENTREX ALLERGEN DISC
    K924119 VENTREX ALLERGEN DISC