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

    FOCISCAN ECHOVISOR SYSTEM

    K Number: K781348 · Decision Oct 3, 1978
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    4
    Review Days
    57

    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
    FOCISCAN ECHOVISOR SYSTEM
    K Number
    K781348
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Metrix Teknika, Inc.
    Date Received
    August 7, 1978
    Decision Date
    October 3, 1978
    Advisory Committee
    Unknown
    Review Advisory Committee
    OB
    Third Party
    N

    Other Clearances by Metrix Teknika, Inc.

    K Number Device Name
    K781803 FILTER, EYRPUR DISPOSABLE LEUKOCITE
    K781802 WASHER SYSTEM, MICROELISA
    K780035 MINIVISOR