Air Compression Leg Massager (Models: S9036C, S9036B and S9036A)
K-Number: K222206 · 2022-09-30
Device Summary
Frequently Asked Questions
What is the Air Compression Leg Massager (Models: S9036C, S9036B and S9036A)?
Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) is a medical device that received FDA 510(k) clearance on 2022-09-30. The listed applicant is Shenzhen Dongjilian Medical Tech Co., Ltd.. The 510(k) number is K222206.
When did Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) receive FDA 510(k) clearance?
Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) received FDA 510(k) clearance on 2022-09-30, under 510(k) number K222206.
Who is the listed applicant for Air Compression Leg Massager (Models: S9036C, S9036B and S9036A)?
The FDA 510(k) record lists Shenzhen Dongjilian Medical Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Air Compression Leg Massager (Models: S9036C, S9036B and S9036A)?
The FDA product code for Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) is IRP.
Other records listing Shenzhen Dongjilian Medical Tech 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.