QXN
- 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.
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| DEN250012 | 2026-03-04 | Lifevac, LLC | LifeVac | — |
Official FDA classification page: QXN
Classification and pathway per current FDA publications. Data from openFDA (CC0).