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

    MAGNETIC RETENTION UNIT

    K Number: K811237 · Decision Jun 16, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    6
    Applicant Total
    1
    Review Days
    43

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    Basic Information

    Device Name
    MAGNETIC RETENTION UNIT
    K Number
    K811237
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.6710
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Universiti Malaya
    Date Received
    May 4, 1981
    Decision Date
    June 16, 1981
    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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