# K030437: Relaxor Perfect Touch Air Massaging System

- Pathway: 510(k) (Traditional)
- Applicant: Salton, Inc.
- Decided: Apr 10, 2003 after 59 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.
59 later devices descend from it; 7 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)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K071596: Potable Air Massager Putifino, Model AM-7 (2008), 55 descendants of its own
- 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

## Indications for use
The Perfect Touch™ Air Massaging System 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 Perfect Touch™ simulates kneading and stroking of tissues by using an inflatable garment.

Source page: https://510kreport.com/device/K030437
Methodology: https://510kreport.com/methodology