QOXNot classified

Multi-Patient Circuit Connector

Unknown

QOX is the FDA product code for Multi-Patient Circuit Connector. FDA's definition for this code reads: "Accessory to single patient ventilator to allow multi-patient ventilation during declared public health emergency". As of 2026-09-10, FDA records hold no 510(k) clearances under this code and no recalls.

Classification record

Product code: QOX
Device name: Multi-Patient Circuit Connector
FDA definition: Accessory to single patient ventilator to allow multi-patient ventilation during declared public health emergency
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: 0

Companies listing this code with FDA

Companies whose registered establishments list this code

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

Recent clearances

Product code QOX

FDA records hold no clearances under product code QOX.

Recent recalls

Product code QOX

FDA records show no recalls under product code QOX.

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)