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

    MSI BONE MARROW BIOPSY NEEDLE W/J TIP

    K Number: K810248 · Decision Mar 20, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    321
    Registration Numbers
    322
    Same Product Code
    106
    Applicant Total
    2
    Review Days
    50

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    Basic Information

    Device Name
    MSI BONE MARROW BIOPSY NEEDLE W/J TIP
    K Number
    K810248
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Creative Research and Mfg., Inc.
    Date Received
    January 29, 1981
    Decision Date
    March 20, 1981
    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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    Other Clearances by Creative Research and Mfg., Inc.

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