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FDA 510(k)

Air Pressure Therapy System: VU-IPC06

K-Number: K210967 · 2021-05-11

Decision Date2021-05-11
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Air Pressure Therapy System: VU-IPC06 is the device name listed in this FDA 510(k) record. The listed applicant is Xiamen Weiyou Intelligent Technology Co., Ltd.. It received FDA 510(k) clearance on 2021-05-11 under 510(k) number K210967. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Air Pressure Therapy System: VU-IPC06?

Air Pressure Therapy System: VU-IPC06 is a medical device that received FDA 510(k) clearance on 2021-05-11. The listed applicant is Xiamen Weiyou Intelligent Technology Co., Ltd.. The 510(k) number is K210967.

When did Air Pressure Therapy System: VU-IPC06 receive FDA 510(k) clearance?

Air Pressure Therapy System: VU-IPC06 received FDA 510(k) clearance on 2021-05-11, under 510(k) number K210967.

Who is the listed applicant for Air Pressure Therapy System: VU-IPC06?

The FDA 510(k) record lists Xiamen Weiyou Intelligent Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Air Pressure Therapy System: VU-IPC06?

The FDA product code for Air Pressure Therapy System: VU-IPC06 is IRP.

Other records listing Xiamen Weiyou Intelligent 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.

View all 7 devices →

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

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