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

    CLIP APPLYING FORCEPS

    K Number: K833651 · Decision Nov 29, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    9
    Registration Numbers
    9
    Same Product Code
    13
    Applicant Total
    22
    Review Days
    41

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    Basic Information

    Device Name
    CLIP APPLYING FORCEPS
    K Number
    K833651
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.4175
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Applicant
    Advanced Biosearch Assn.
    Date Received
    October 19, 1983
    Decision Date
    November 29, 1983
    Product Code
    HCI
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    HCI Applier, Aneurysm Clip

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