K-number	K233536
Device name	Air Compression Recovery System
Applicant	Shenzhen Dongjilian Medical Tech Co., Ltd.
Product code	IRP
Device class	Class II
Decision date	Dec 16, 2023
Decision	Substantially Equivalent
Regulation	890.5650

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Source

View the full FDA submission: accessdata.fda.gov

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Air Compression Recovery System

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