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FDA 510(k)

Air Compression Leg Massager (Models: S9036C, S9036B and S9036A)

K-Number: K222206 · 2022-09-30

ApplicantShenzhen Dongjilian Medical Tech Co., Ltd.
Decision Date2022-09-30
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) is a medical device manufactured by Shenzhen Dongjilian Medical Tech Co., Ltd.. It received FDA 510(k) clearance on 2022-09-30 under approval number K222206. 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 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. It is manufactured by Shenzhen Dongjilian Medical Tech Co., Ltd.. The 510(k) number is K222206.

When was Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) approved by the FDA?

Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) received FDA 510(k) clearance on 2022-09-30, under approval number K222206.

What company makes Air Compression Leg Massager (Models: S9036C, S9036B and S9036A)?

Air Compression Leg Massager (Models: S9036C, S9036B and S9036A) is manufactured by Shenzhen Dongjilian Medical Tech Co., Ltd..

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 Devices by Shenzhen Dongjilian Medical Tech Co., Ltd.

K233536Air Compression Recovery System

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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.

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