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High Flow/High Velocity Humidified Oxygen Delivery Device
FDA product code QAV · Class 2 · Anesthesiology
143
Registered devices
38
Adverse events
1
Recalls
3
510(k) clearances
Devices with this code
Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.F&P Airvo 3 — FISHER & PAYKEL HEALTHCARE LIMITEDFisher & Paykel Healthcare — FISHER & PAYKEL HEALTHCARE LIMITEDVapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.F&P Airvo 3 — FISHER & PAYKEL HEALTHCARE LIMITEDVapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.Vapotherm — VAPOTHERM, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-08-07 | Fisher & Paykel Healthcare, Ltd. | Due to a software issue, affected devices that are set up with High Pressure Oxygen (HPO), if the flow alignment alarm occurs, the device will deliver room air |
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