# K071596: Potable Air Massager Putifino, Model AM-7

- Pathway: 510(k) (Traditional)
- Applicant: Nihon Seimitsu Sokki Co., Ltd.
- Decided: Feb 15, 2008 after 248 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: 3 generations back to K850316 (1985). 4 ancestors in all.
55 later devices descend from it; 2 cite it directly.
0 of 60 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050697: Model DS-1901 Digital Blood Pressure Monitor, Nihon Seimitsu Sokki Co., Ltd. (2005) Summary page 1.
- K030437: Relaxor Perfect Touch Air Massaging System, Salton, Inc. (2003) Summary page 3.

## Most influential descendants
- K092435: Verseo Air Pressure Massager (2010), 54 descendants of its own
- 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

## Indications for use
The Portable Air Massager putifino AM-7 is indicated for the temporary relief of minor muscle aches and pains and for temporary increase in circulation to the treated areas in people who are in good health. The Portable Air Massager putifino AM-7 simulates kneading and stroking of tissues by using an inflatable garment (Cuff).

Source page: https://510kreport.com/device/K071596
Methodology: https://510kreport.com/methodology