510(k) K221841 · BTM Ventilator, Emergency, Manual (Resuscitator)
EOlife®
| Applicant | Archeon, Besançon, FR |
| Decision | Substantially Equivalent, Mar 18, 2023 |
| Received | Jun 24, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221841
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.