QOSNot classified

Continuous Ventilator

Unknown

QOS is the FDA product code for Continuous Ventilator. FDA's definition for this code reads: "Intended to provide continuous ventilatory support for use during declared public health emergency. May be used in hospital or facility settings". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and one recall.

Classification record

Product code: QOS
Device name: Continuous Ventilator
FDA definition: Intended to provide continuous ventilatory support for use during declared public health emergency. May be used in hospital or facility settings.
Device class: Not classified
Review panel: Unknown
Submission type: FDA code 8
Implant: No
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 0
Ingested recalls: 1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code QOS.

Recent clearances

Product code QOS

FDA records hold no clearances under product code QOS.

Recent recalls

Product code QOS

Z-1775-2022Class IIMedtronic has confirmed six reports from customers outside the US where the ventilator became inoperable due to loss of gas...Covidien Llc / initiated 2022-08-19 / 5 US

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)