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

    MORWEL CANNULA

    K Number: K831520 · Decision Jun 20, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    4
    Review Days
    39

    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
    MORWEL CANNULA
    K Number
    K831520
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Morwel Corp.
    Date Received
    May 12, 1983
    Decision Date
    June 20, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N

    Other Clearances by Morwel Corp.

    K Number Device Name
    K962525 ULTRA-SAFE ULTRASONIC ASPIRATOR SYSTEM
    K841160 MORWEL ASPIRATOR
    K841159 SUCTION TIPS