Air Compression Therapy Device
K-Number: K201694 · 2020-11-19
Device Summary
Frequently Asked Questions
What is the Air Compression Therapy Device?
Air Compression Therapy Device is a medical device that received FDA 510(k) clearance on 2020-11-19. The listed applicant is Shenzhen Dongjilian Electronics Co., Ltd.. The 510(k) number is K201694.
When did Air Compression Therapy Device receive FDA 510(k) clearance?
Air Compression Therapy Device received FDA 510(k) clearance on 2020-11-19, under 510(k) number K201694.
Who is the listed applicant for Air Compression Therapy Device?
The FDA 510(k) record lists Shenzhen Dongjilian Electronics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Air Compression Therapy Device?
The FDA product code for Air Compression Therapy Device is IRP.
Other records listing Shenzhen Dongjilian Electronics 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.