Product code QAV— Anesthesiology
F&P Airvo 3
- Classification name
- High Flow/High Velocity Humidified Oxygen Delivery Device
- Device class
- Class 2
- Regulation
- 21 CFR 868.5454
- Advisory panel
- Anesthesiology
- Total cleared
- 3
- First cleared
- Most recent
FDA classification definition
“Intended to deliver high flow and/or high velocity oxygen with humidification.”
Market context for product code QAV
FDA has cleared devices under product code QAV between 2018 and 2023, filed by 2 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.
Clearances per year
- 2023
- 2022
- 2018
Top applicants under product code QAV
Adverse events under product code QAV
product code QAV- Death
- 3
- Total
- 3
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Recent clearances under product code QAV
Data sourced from openFDA. This site is unofficial and independent of the FDA.