BEUDAMED
    FDA 510(k) FDA unclassified Substantially Equivalent 🇨🇦 Canada

    METRICOM

    K Number: K860225 · Decision Feb 11, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    1
    Registration Numbers
    1
    Same Product Code
    7
    Applicant Total
    2
    Review Days
    20

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    Basic Information

    Device Name
    METRICOM
    K Number
    K860225
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    Far Orthopedics, Inc.
    Date Received
    January 22, 1986
    Decision Date
    February 11, 1986
    Product Code
    LDK
    Advisory Committee
    Unknown
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LDK Device, Sensing, Optical Contour

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    Other Clearances by Far Orthopedics, Inc.

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