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

    DISPO-URETTE

    K Number: K860796 · Decision Apr 8, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    6
    Registration Numbers
    6
    Same Product Code
    4
    Applicant Total
    2
    Review Days
    35

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    Basic Information

    Device Name
    DISPO-URETTE
    K Number
    K860796
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    884.1050
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    Roland J. Zwick, Inc.
    Date Received
    March 4, 1986
    Decision Date
    April 8, 1986
    Product Code
    PCF
    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
    PCF Sampler, Endocervical

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    Other Clearances by Roland J. Zwick, Inc.

    K Number Device Name
    K840352 CIN-SHEAR