510(k) K222292 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
F&P myAirvo 3
| Applicant | Fisher & Paykel Healthcare, Manukau, NZ |
| Decision | Substantially Equivalent, May 8, 2024 |
| Received | Jul 29, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222292
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.