510(k) K231956 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
F&P Optiflow+ Duet Nasal Cannula
| Applicant | Fisher & Paykel Healthcare, Ltd., Auckland, NZ |
| Decision | Substantially Equivalent, Feb 7, 2024 |
| Received | Jul 3, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231956
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.