BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    AIRLIFE DEMAND NASAL CANNULA

    K Number: K023673 · Decision May 2, 2003
    View on FDA
    Classifications
    1
    FEI Numbers
    17
    Registration Numbers
    17
    Same Product Code
    70
    Applicant Total
    63
    Review Days
    182

    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
    AIRLIFE DEMAND NASAL CANNULA
    K Number
    K023673
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5905
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Allegiance Healthcare Corp.
    Date Received
    November 1, 2002
    Decision Date
    May 2, 2003
    Product Code
    NFB
    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
    NFB Conserver, Oxygen

    Similar 510(k) Clearances

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

    Respond OC Conserving Regulator (130-0800)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Proxima

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Effortless Oxygen Conserver System Models Effortless Pro and Effortless Mobile

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Apogee

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen Cannula

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMEN

    FDA 510(k)
    FDA Class 2 ·Anesthesiology
    View all

    Other Clearances by Allegiance Healthcare Corp.

    K Number Device Name
    K023419 TRILAMINATE DRAPES/TIBURON
    K024120 MODIFICATION TO TEMNO BIOPSY NEEDLES
    K024292 MODIFICATION TO POSITIVE TOUCH POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN AND CHEMOTHERAPY LABELING CLAIM
    K024102 DENTAL POWDER-FREE LATEX EXAMINATION GLOVES WITH PROTEIN LABELING CLAIM
    K023425 DRAPES WITH ABSORBENT REINFORCEMENT
    K022765 NITRILE POWDER-FREE EXAMINATION GLOVES
    K023170 NITRILE POWDER-FREE EXAMINATION GLOVES
    K023167 BREATHABLE SURGICAL GOWN
    K012931 GENESIS STERRAD COMPATIBLE REUSABLE STERILIZATION CONTAINER SYSTEM
    K020818 POWDER-FREE LATEX EXAMINATION GLOVES WITH COLORANTS
    Search all 63 clearances from Allegiance Healthcare Corp. →