BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    MASTERSTIM I-2

    K Number: K924490 · Decision Feb 5, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    46
    Registration Numbers
    46
    Same Product Code
    72
    Applicant Total
    2
    Review Days
    155

    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
    MASTERSTIM I-2
    K Number
    K924490
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    882.5890
    Medical Specialty
    Neurology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Health Care Assoc.
    Date Received
    September 3, 1992
    Decision Date
    February 5, 1993
    Product Code
    LIH
    Advisory Committee
    Neurology
    Review Advisory Committee
    NE
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LIH Interferential Current Therapy

    Similar 510(k) Clearances

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

    Vecttor VT-300

    FDA 510(k)
    FDA Class 2 ·Neurology

    ETD4000

    FDA 510(k)
    FDA Class 2 ·Neurology

    Avid IF2

    FDA 510(k)
    FDA Class 2 ·Neurology

    GEMORE TRUE SINE INTERFERENTIAL STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    VECTTOR VT-200

    FDA 510(k)
    FDA Class 2 ·Neurology

    EVERYWAY INTERFERNTIAL STIMULATOR, MODEL IF-908

    FDA 510(k)
    FDA Class 2 ·Neurology
    View all

    Other Clearances by Health Care Assoc.

    K Number Device Name
    K932075 MASTERSTIM 1-4