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

    GELSPHERES / BEADBLOCK COMPRESSIBLE MICROSPHERES

    K Number: K033761 · Decision Feb 4, 2004
    View on FDA
    Classifications
    1
    FEI Numbers
    60
    Registration Numbers
    60
    Same Product Code
    179
    Applicant Total
    4
    Review Days
    64

    Basic Information

    Device Name
    GELSPHERES / BEADBLOCK COMPRESSIBLE MICROSPHERES
    K Number
    K033761
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.5950
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    BIOCOMPATIBLES U.K. LIMITED
    Date Received
    December 2, 2003
    Decision Date
    February 4, 2004
    Product Code
    HCG
    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
    HCG Device, Neurovascular Embolization

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    Other Clearances by BIOCOMPATIBLES U.K. LIMITED

    K Number Device Name
    K094018 LC BEAD MICROSPHERES, BEAD BLOCK COMPRESSIBLE MICROSPHERES
    K083091 LC BEAD MICROSPHERES, BEAD BLOCK COMPRESSIBLE MICROSPHERES
    K042231 GELSPHERES MICROSPHERES AND BEAD BLOCK COMPRESSIBLE MICROSPHERES