YY-A02-B Overlapped Compression Therapy
K-Number: K221862 · 2022-12-08
Device Summary
Frequently Asked Questions
What is the YY-A02-B Overlapped Compression Therapy?
YY-A02-B Overlapped Compression Therapy is a medical device that received FDA 510(k) clearance on 2022-12-08. The listed applicant is Huizhou Xinyi Technology Co., Ltd.. The 510(k) number is K221862.
When did YY-A02-B Overlapped Compression Therapy receive FDA 510(k) clearance?
YY-A02-B Overlapped Compression Therapy received FDA 510(k) clearance on 2022-12-08, under 510(k) number K221862.
Who is the listed applicant for YY-A02-B Overlapped Compression Therapy?
The FDA 510(k) record lists Huizhou Xinyi Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for YY-A02-B Overlapped Compression Therapy?
The FDA product code for YY-A02-B Overlapped Compression Therapy is IRP.
Other records listing Huizhou Xinyi Technology 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.