QXN

Suction Anti-Choking Device As A Second-Line Treatment

Product code
QXN
Device name
Suction Anti-Choking Device As A Second-Line Treatment
Device class
Class 2
21 CFR
21 CFR 874.5400
Medical specialty
Ear, Nose, Throat
Marketing pathway
510(K)
Flag
Life-sustaining / life-supporting
510(k) clearances (last 3 years)
1
Summaries archived here
0 (direct download)
510(k) clearances (all years, FDA)
1 (all years; only the last 3 years are listed here)

FDA classification definition

A suction anti-choking device as a second-line treatment is intended to be used, by application of suction, to resolve choking in victims experiencing complete airway obstruction. The device is intended to be used as a second-line treatment in an emergency situation after unsuccessful use of a basic life support (BLS) choking protocol.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2026-03-04.

NumberDecision dateApplicantDevice nameSummary
DEN2500122026-03-04Lifevac, LLCLifeVac
Official FDA classification page: QXN
Classification and pathway per current FDA publications. Data from openFDA (CC0).