510(k) DEN250012 ยท QXN Suction Anti-Choking Device As A Second-Line Treatment
LifeVac
| Applicant | Lifevac, LLC, Nesconset NY, US |
| Decision | Unknown, Mar 4, 2026 |
| Received | Apr 11, 2025 |
| Type | Direct |
| FDA record | Open on fda.gov |
Recalls that name DEN250012
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.