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

    POST-AID

    K Number: K840907 · Decision Aug 2, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    21
    Registration Numbers
    21
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    156

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    Basic Information

    Device Name
    POST-AID
    K Number
    K840907
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    874.5220
    Medical Specialty
    Ear, Nose, Throat
    Decision
    Substantially Equivalent
    Applicant
    E.W. Link, Inc.
    Date Received
    February 28, 1984
    Decision Date
    August 2, 1984
    Product Code
    KCM
    Advisory Committee
    Ear, Nose, Throat
    Review Advisory Committee
    EN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    KCM Dropper, Ent