F&P Airvo 3
K-Number: K221338 · 2023-01-27
ApplicantFisher & Paykel Healthcare
Decision Date2023-01-27
Product CodeQAV
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
F&P Airvo 3 is a medical device manufactured by Fisher & Paykel Healthcare. It received FDA 510(k) clearance on 2023-01-27 under approval number K221338. The device is classified under product code QAV. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the F&P Airvo 3?
F&P Airvo 3 is a medical device that received FDA 510(k) clearance on 2023-01-27. It is manufactured by Fisher & Paykel Healthcare. The 510(k) number is K221338.
When was F&P Airvo 3 approved by the FDA?
F&P Airvo 3 received FDA 510(k) clearance on 2023-01-27, under approval number K221338.
What company makes F&P Airvo 3?
F&P Airvo 3 is manufactured by Fisher & Paykel Healthcare.
What is the FDA product code for F&P Airvo 3?
The FDA product code for F&P Airvo 3 is QAV.
Other Devices by Fisher & Paykel Healthcare
Related Devices (Code: QAV)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.