# K092435: Verseo Air Pressure Massager

- Pathway: 510(k) (Traditional)
- Applicant: The American Export Group & International Services
- Decided: Mar 9, 2010 after 214 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: 4 generations back to K850316 (1985). 6 ancestors in all.
54 later devices descend from it; 1 cites it directly.
0 of 61 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K040905: Wellness/Jolivete, Tohkai Precision Ind., Ltd. (2005) Summary page 2.
- K030437: Relaxor Perfect Touch Air Massaging System, Salton, Inc. (2003) Summary page 2.
- K071596: Potable Air Massager Putifino, Model AM-7, Nihon Seimitsu Sokki Co., Ltd. (2008) Summary page 2.

## Most influential descendants
- K122154: Powerplay Muscle Massager (2012), 53 descendants of its own
- K160608: NormaTec Pulse and NormaTec Pulse Pro (2016), 51 descendants of its own
- K182668: Rapid Reboot Compression Therapy System (2018), 38 descendants of its own
- K193354: Air Compression Therapy Device (2020), 20 descendants of its own
- K183169: Pulse 2.0, Pulse Pro 2.0 (2018), 10 descendants of its own

## Indications for use
The Versec Air Pressure Massager is intended to temporarily relieve minor muscle aches and pains and to temporarily increase circulation to the treated areas. The Verseo Air Pressure Massager simulates kneading and stroking of tissues with the hands by use of an inflatable pressure cuff.

Source page: https://510kreport.com/device/K092435
Methodology: https://510kreport.com/methodology