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

    TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE

    K Number: K901239 · Decision May 15, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    89
    Registration Numbers
    89
    Same Product Code
    260
    Applicant Total
    5
    Review Days
    61

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    Basic Information

    Device Name
    TELEDYNE GETZ'S DISPOSABLE PROPHY ANGLE
    K Number
    K901239
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4200
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Teledyne Getz
    Date Received
    March 15, 1990
    Decision Date
    May 15, 1990
    Product Code
    EFB
    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
    EFB Handpiece, Air-Powered, Dental

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    Other Clearances by Teledyne Getz

    K Number Device Name
    K923675 DENSPRO MEDIUM MINT PROPHY PASTE
    K923674 DENSPRO COARSE MINT PROPHY PASTE
    K903568 SUPER STRENGTH DENTURE ADHESIVE CREAM
    K901938 SUPER STRENGTH DENTURE ADHESIVE CREAM