RXiBreeze PAP System (RXiBreeze 20C)
K-Number: K253044 · 2026-07-23
Device Summary
Frequently Asked Questions
What is the RXiBreeze PAP System (RXiBreeze 20C)?
RXiBreeze PAP System (RXiBreeze 20C) is a medical device that received FDA 510(k) clearance on 2026-07-23. The listed applicant is Resvent Medical Technology Co., Ltd.. The 510(k) number is K253044.
When did RXiBreeze PAP System (RXiBreeze 20C) receive FDA 510(k) clearance?
RXiBreeze PAP System (RXiBreeze 20C) received FDA 510(k) clearance on 2026-07-23, under 510(k) number K253044.
Who is the listed applicant for RXiBreeze PAP System (RXiBreeze 20C)?
The FDA 510(k) record lists Resvent Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RXiBreeze PAP System (RXiBreeze 20C)?
The FDA product code for RXiBreeze PAP System (RXiBreeze 20C) is BZD.
Related Devices (Code: BZD)
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.