Air compression therapy system FO3002
K-Number: K212169 · 2021-11-23
Device Summary
Frequently Asked Questions
What is the Air compression therapy system FO3002?
Air compression therapy system FO3002 is a medical device that received FDA 510(k) clearance on 2021-11-23. The listed applicant is Foshan Hongfeng Co., Ltd.. The 510(k) number is K212169.
When did Air compression therapy system FO3002 receive FDA 510(k) clearance?
Air compression therapy system FO3002 received FDA 510(k) clearance on 2021-11-23, under 510(k) number K212169.
Who is the listed applicant for Air compression therapy system FO3002?
The FDA 510(k) record lists Foshan Hongfeng Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Air compression therapy system FO3002?
The FDA product code for Air compression therapy system FO3002 is IRP.
Other records listing Foshan Hongfeng Co., 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: IRP)
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.