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

    A CALIPER

    K Number: K820659 · Decision Mar 19, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    194
    Registration Numbers
    194
    Same Product Code
    6
    Applicant Total
    6
    Review Days
    9

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    Basic Information

    Device Name
    A CALIPER
    K Number
    K820659
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    888.4150
    Medical Specialty
    Orthopedic
    Decision
    Substantially Equivalent
    Applicant
    Twin City Surgical, Inc.
    Date Received
    March 10, 1982
    Decision Date
    March 19, 1982
    Product Code
    KTZ
    Advisory Committee
    Orthopedic
    Review Advisory Committee
    OR
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KTZ Caliper

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