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

    NEY EQUI-HINGE

    K Number: K790290 · Decision Apr 10, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    6
    Applicant Total
    46
    Review Days
    61

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    Basic Information

    Device Name
    NEY EQUI-HINGE
    K Number
    K790290
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.6710
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Deringer-Ney, Inc.
    Date Received
    February 8, 1979
    Decision Date
    April 10, 1979
    Product Code
    ECG
    Advisory Committee
    Dental
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    ECG Sterilizer, Boiling Water

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