Air Compression Recovery System
K-Number: K233536 · 2023-12-16
Device Summary
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. The listed applicant is Shenzhen Dongjilian Medical Tech Co., Ltd.. The 510(k) number is K233536.
When did Air Compression Recovery System receive FDA 510(k) clearance?
Air Compression Recovery System received FDA 510(k) clearance on 2023-12-16, under 510(k) number K233536.
Who is the listed applicant for Air Compression Recovery System?
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 Recovery System?
The FDA product code for Air Compression Recovery System 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.