# K242615: Intermittent pressure compression system (Compression Pump PT1005A; Leg Compression Cuffs; L-1001S, L-1001L, L-1001XL, L-1001XXL, L-1001XXXL)

- Pathway: 510(k) (Traditional)
- Applicant: Xiamen Taotao Technology Co., Ltd.
- Decided: Jul 23, 2025 after 323 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
Longest line of descent: 1 generation back to K243320 (2024). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K243320: Air Pressure Therapy System (VU-IPC04B), Xiamen Weiyou Intelligent Technology Co., Ltd. (2024). Cleared while this submission was under review Summary page 5.

## Indications for use
The device is intended to temporarily relieve minor muscle aches and/or pains, and to temporarily increase circulation to the treated areas in people who are in good health.

Source page: https://510kreport.com/device/K242615
Methodology: https://510kreport.com/methodology