510(k) K220703 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
F&P 950 Respiratory Humidifier
| Applicant | Fisher & Paykel Healthcare, Manukau, NZ |
| Decision | Substantially Equivalent, Jun 16, 2023 |
| Received | Mar 10, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K220703
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.