BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

    ACME SURGICAL FACE MASK WITH EAR-LOOP MODEL YN-501 AB/W/G/P

    K Number: K123115 · Decision May 20, 2013
    View on FDA
    Classifications
    1
    FEI Numbers
    315
    Registration Numbers
    315
    Same Product Code
    606
    Applicant Total
    1
    Review Days
    229

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    Basic Information

    Device Name
    ACME SURGICAL FACE MASK WITH EAR-LOOP MODEL YN-501 AB/W/G/P
    K Number
    K123115
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4040
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Acme Filter Mask, Inc.
    Date Received
    October 3, 2012
    Decision Date
    May 20, 2013
    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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