# K251623: Air Compression Therapy Device (K1002/K1006/K1007/K1008/K1061)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Yicai Health Technology Co., Ltd.
- Decided: Sep 17, 2025 after 112 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 therapy device(K1002K1002/K1006/K1007/K1008/K1061 ) is an air pressure massager intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas.

Source page: https://510kreport.com/device/K251623
Methodology: https://510kreport.com/methodology