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

    ANSPACH LEG SUPPORT

    K Number: K801330 · Decision Jun 26, 1980
    View on FDA
    Classifications
    1
    FEI Numbers
    279
    Registration Numbers
    280
    Same Product Code
    7
    Applicant Total
    60
    Review Days
    23

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    Basic Information

    Device Name
    ANSPACH LEG SUPPORT
    K Number
    K801330
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.6820
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    The Anspach Effort, Inc.
    Date Received
    June 3, 1980
    Decision Date
    June 26, 1980
    Product Code
    CCX
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    CCX Support, Patient Position

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