F&P 820 Humidification System
K-Number: K223684 · 2023-09-05
Device Summary
Frequently Asked Questions
What is the F&P 820 Humidification System?
F&P 820 Humidification System is a medical device that received FDA 510(k) clearance on 2023-09-05. The listed applicant is Fisher & Paykel Healthcare, Ltd.. The 510(k) number is K223684.
When did F&P 820 Humidification System receive FDA 510(k) clearance?
F&P 820 Humidification System received FDA 510(k) clearance on 2023-09-05, under 510(k) number K223684.
Who is the listed applicant for F&P 820 Humidification System?
The FDA 510(k) record lists Fisher & Paykel Healthcare, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for F&P 820 Humidification System?
The FDA product code for F&P 820 Humidification System is BTT.
Other records listing Fisher & Paykel Healthcare, Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: BTT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.