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

    DEVILBISS AP-50 COMPRESSOR/NEBULIZER

    K Number: K900602 · Decision Apr 23, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    108
    Registration Numbers
    108
    Same Product Code
    220
    Applicant Total
    29
    Review Days
    74

    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
    DEVILBISS AP-50 COMPRESSOR/NEBULIZER
    K Number
    K900602
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5450
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Devilbiss Health Care, Inc.
    Date Received
    February 8, 1990
    Decision Date
    April 23, 1990
    Product Code
    BTT
    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
    BTT Humidifier, Respiratory Gas, (Direct Patient Interface)

    Similar 510(k) Clearances

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

    HVT 2.0

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    FL-10000U Respiratory Humidifier

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Laboratorios Biogalenic Sterile Water for Inhalation, USP

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Optiflow Switch+ Filtered Nasal Interface with CO2 Sampling (AA042J)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Hudson RCI® Comfort Flo Nasal Cannula Premature, Infant; Hudson RCI® Comfort Flo Plus and Soft Plus Cannula Extra Small

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Optiflow+ Nasal Cannula - Small (OPT942); Optiflow+ Nasal Cannula - Medium (OPT944); Optiflow+ Nasal Cannula - Large (OPT946); Optiflow+ Nasal Cannula Small (MYOPT9SMALL); Optiflow+ Nasal Cannula Medium (MYOPT9MEDIUM); Optiflow+ Nasal Cannula Large (MYOPT9LARGE)

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

    Other Clearances by Devilbiss Health Care, Inc.

    K Number Device Name
    K963349 DEVILBISS 8650D
    K970289 COMPRESSOR/NEBULIZER #3650
    K961126 PULSE DOSE SERIES
    K950849 MODEL #7354
    K952491 MODEL 7355
    K952249 JET NEBULIZER
    K953815 5 LPM OXYGEN CONCENTRATOR
    K952037 3 LPM OXYGEN CONCENTRATOR
    K946095 DEVILBISS MODEL 5500
    K944611 MODEL# 7500 SURVEYOR
    Search all 29 clearances from Devilbiss Health Care, Inc. →