BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    M.D.I. ADAPTER

    K Number: K895549 · Decision Nov 21, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    167
    Registration Numbers
    167
    Same Product Code
    93
    Applicant Total
    1
    Review Days
    69

    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
    M.D.I. ADAPTER
    K Number
    K895549
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.5810
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Custom Connection Corp.
    Date Received
    September 13, 1989
    Decision Date
    November 21, 1989
    Product Code
    BZA
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    BZA Connector, Airway (Extension)

    Similar 510(k) Clearances

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

    TRACH-ASSIST

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    SURELOC CIRCUIT CONNECTOR

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    DISPOSABLE FLEX TUBE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    UNICOR, INC. CONNECTORS & AIRWAY EXTENSIONS

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    NEO-LINK, DISPOSABLE NEONATAL AIR WAY CONNECTOR

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    DISPOSABLE AIRWAY CONNECTORS FOR GAS SAMPLING

    FDA 510(k)
    FDA Class 1 ·Anesthesiology
    View all