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

    Medifun Safety Lancet ( MSL1 series)

    K Number: K241750 · Decision Aug 15, 2024
    View on FDA
    Classifications
    1
    FEI Numbers
    157
    Registration Numbers
    157
    Same Product Code
    109
    Applicant Total
    2
    Review Days
    58

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    Basic Information

    Device Name
    Medifun Safety Lancet ( MSL1 series)
    K Number
    K241750
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    878.4850
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Medifun Corporation
    Date Received
    June 18, 2024
    Decision Date
    August 15, 2024
    Product Code
    FMK
    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
    FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

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