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

    NASSAL PRESSURE/FLOW RECORDER

    K Number: K772193 · Decision Dec 2, 1977
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    3
    Applicant Total
    1
    Review Days
    4

    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
    NASSAL PRESSURE/FLOW RECORDER
    K Number
    K772193
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Adco Labs.
    Date Received
    November 28, 1977
    Decision Date
    December 2, 1977
    Product Code
    ETL
    Advisory Committee
    Unknown
    Review Advisory Committee
    EN
    Third Party
    N

    Similar 510(k) Clearances

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

    ATMOS ENT PATIENT CHAIR #1

    FDA 510(k)

    ATMOS ENT PATIENT CHAIR #5

    FDA 510(k)

    ANEMOMETER, NASAL, EXETER

    FDA 510(k)