# K122154: Powerplay Muscle Massager

- Pathway: 510(k) (Traditional)
- Applicant: Fig, LLC
- Decided: Nov 21, 2012 after 124 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: 5 generations back to K850316 (1985). 7 ancestors in all.
53 later devices descend from it; 3 cite 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)
- K092435: Verseo Air Pressure Massager, The American Export Group & International Services (2010) Summary page 2.
- K071596: Potable Air Massager Putifino, Model AM-7, Nihon Seimitsu Sokki Co., Ltd. (2008) Summary page 2.
- K030437: Relaxor Perfect Touch Air Massaging System, Salton, Inc. (2003) Summary page 2.

## Most influential descendants
- 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
- K220217: Normatec 3 (2022), 7 descendants of its own

## Indications for use
The PowerPlay model PPRT-01 is intended to be an over-the-counter portable inflatable tube massage system which simulates kneading and stroking of tissue with the hands by use of inflatable pressure cuffs. This device can be used to: * Temporarily increase blood circulation in the treated areas; * Temporary relief of minor muscle aches and pains.

Source page: https://510kreport.com/device/K122154
Methodology: https://510kreport.com/methodology