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

    INNOSCAN EXAMINATION LIGHT

    K Number: K827796 · Decision Aug 24, 1982
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    3
    Review Days
    26

    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
    INNOSCAN EXAMINATION LIGHT
    K Number
    K827796
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Innomed Corp.
    Date Received
    July 29, 1982
    Decision Date
    August 24, 1982
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

    Other Clearances by Innomed Corp.

    K Number Device Name
    K872747 LASER CENTERING DEVICE
    K822574 INNOMED PD-1 KIT