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

    BUSSE ISOLATION AND PROCEDURAL MASKS

    K Number: K940720 · Decision Nov 2, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    315
    Registration Numbers
    315
    Same Product Code
    606
    Applicant Total
    31
    Review Days
    257

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    Basic Information

    Device Name
    BUSSE ISOLATION AND PROCEDURAL MASKS
    K Number
    K940720
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4040
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Busse Hospital Disposables, Inc.
    Date Received
    February 18, 1994
    Decision Date
    November 2, 1994
    Product Code
    FXX
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FXX Mask, Surgical

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