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

    ANCHOR BIOPSY NEEDLE

    K Number: K873124 · Decision Sep 8, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    321
    Registration Numbers
    322
    Same Product Code
    106
    Applicant Total
    7
    Review Days
    29

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    Basic Information

    Device Name
    ANCHOR BIOPSY NEEDLE
    K Number
    K873124
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Anchor Products Co.
    Date Received
    August 10, 1987
    Decision Date
    September 8, 1987
    Product Code
    GAA
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GAA Needle, Aspiration And Injection, Disposable

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    K884862 ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADE
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