BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    EVER-SHARP BIOPSY FORCEPS

    K Number: K895303 · Decision Jan 16, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    160
    Registration Numbers
    160
    Same Product Code
    21
    Applicant Total
    2
    Review Days
    140

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    Basic Information

    Device Name
    EVER-SHARP BIOPSY FORCEPS
    K Number
    K895303
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    884.4530
    Medical Specialty
    Obstetrics/Gynecology
    Decision
    Substantially Equivalent
    Applicant
    Southwest Medical Mfg., Inc.
    Date Received
    August 29, 1989
    Decision Date
    January 16, 1990
    Product Code
    HFB
    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
    HFB Forceps, Biopsy, Gynecological

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    Other Clearances by Southwest Medical Mfg., Inc.

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