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

    SPRINT S-2 INSTRU. CENTER (MODEL 92329)

    K Number: K770129 · Decision Jan 28, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    69
    Registration Numbers
    69
    Same Product Code
    60
    Applicant Total
    2
    Review Days
    7

    Research this 510(k) in seconds

    The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

    Free to try · every answer cites its records

    Ask the Research Assistant See examples

    Basic Information

    Device Name
    SPRINT S-2 INSTRU. CENTER (MODEL 92329)
    K Number
    K770129
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4200
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Chemetron Health Systems
    Date Received
    January 21, 1977
    Decision Date
    January 28, 1977
    Product Code
    EBW
    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
    EBW Controller, Foot, Handpiece And Cord

    Similar 510(k) Clearances

    Other 510(k) clearances with the same product code (EBW), ordered by most recent decision date.

    Motor Handpiece and Control Unit (SDI10)

    FDA 510(k)
    FDA Class 1 ·Dental

    Star E900 Electric System

    FDA 510(k)
    FDA Class 1 ·Dental

    Motor and Apex Module (MaAM)

    FDA 510(k)
    FDA Class 1 ·Dental

    ELEC ENGINE (Model: ISE-170L)

    FDA 510(k)
    FDA Class 1 ·Dental

    Dental Implant Unit

    FDA 510(k)
    FDA Class 1 ·Dental

    NLZ Built-In Motor System

    FDA 510(k)
    FDA Class 1 ·Dental
    View all

    Other Clearances by Chemetron Health Systems

    K Number Device Name
    K760228 ANESTHESIA MACHINE, CHEMETRON