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

    3M(TM) SURGICAL SLIPPER, 9660 SERIES

    K Number: K946162 · Decision Jan 24, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    114
    Registration Numbers
    114
    Same Product Code
    3
    Applicant Total
    8
    Review Days
    36

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    Basic Information

    Device Name
    3M(TM) SURGICAL SLIPPER, 9660 SERIES
    K Number
    K946162
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4800
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Wahl Clipper Corp.
    Date Received
    December 19, 1994
    Decision Date
    January 24, 1995
    Product Code
    LWK
    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
    LWK Razor, Surgical

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