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FDA 510(k)

Air Compression Recovery System

K-Number: K233536 · 2023-12-16

ApplicantShenzhen Dongjilian Medical Tech Co., Ltd.
Decision Date2023-12-16
Product CodeIRP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Air Compression Recovery System is a medical device manufactured by Shenzhen Dongjilian Medical Tech Co., Ltd.. It received FDA 510(k) clearance on 2023-12-16 under approval number K233536. 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 Recovery System?

Air Compression Recovery System is a medical device that received FDA 510(k) clearance on 2023-12-16. It is manufactured by Shenzhen Dongjilian Medical Tech Co., Ltd.. The 510(k) number is K233536.

When was Air Compression Recovery System approved by the FDA?

Air Compression Recovery System received FDA 510(k) clearance on 2023-12-16, under approval number K233536.

What company makes Air Compression Recovery System?

Air Compression Recovery System is manufactured by Shenzhen Dongjilian Medical Tech Co., Ltd..

What is the FDA product code for Air Compression Recovery System?

The FDA product code for Air Compression Recovery System is IRP.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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