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

    SURGICAL FACE MASK

    K Number: K802373 · Decision Nov 12, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    315
    Registration Numbers
    315
    Same Product Code
    606
    Applicant Total
    8
    Review Days
    44

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    Basic Information

    Device Name
    SURGICAL FACE MASK
    K Number
    K802373
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4040
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Louis M. Gerson Co., Inc.
    Date Received
    September 29, 1980
    Decision Date
    November 12, 1980
    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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    Other Clearances by Louis M. Gerson Co., Inc.

    K Number Device Name
    K061375 RESPIRATOR N95 PARTICULATE RESPIRATOR, MODEL 1730
    K050193 GERSON 2130/31 TYPE N95 NIOSH CERTIFIED SURGICAL RESPIRATOR
    K960778 ISOLAIR APR TYPE N95
    K925185 ISOLAIR 2 FLUID RESIST SURG/PROCE/CONE/EARLOOP MAS
    K931288 ISOLAIR 2 FULL FACE SPLASH GUARD
    K922507 GERSON ISOLAIR APR PARTICULATE SURGICAL MASK
    K881910 LABELING CHANGE TO SURGICAL FACE MASK