# K233536: Air Compression Recovery System

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Dongjilian Medical Tech Co., Ltd.
- Decided: Dec 16, 2023 after 43 days
- Product code: IRP (Massager, Powered Inflatable Tube)
- Device class: 2
- Regulation: 21 CFR 890.5650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Air Compression Recovery System is intended for the temporary relief of minor muscle aches and pains and for the temporary increase in circulation to the treated areas, it can simulate kneading and stroking of tissues by using an inflatable garment.

Source page: https://510kreport.com/device/K233536
Methodology: https://510kreport.com/methodology