# K032505: Air Press Massager

- Pathway: 510(k) (Traditional)
- Applicant: Telebrands Corp
- Decided: Sep 24, 2003 after 42 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.
53 later devices descend from it; 1 cites it directly.
0 of 54 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
- K112890: Normatec MVP (2012), 52 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 Air Press Massager is indicated for the temporary relief of minor muscle aches and pains and for temporary increase in circulation to the treated areas in people with good health. The Air Press simulates kneading and stroking of tissues by using an inflatable garment.

Source page: https://510kreport.com/device/K032505
Methodology: https://510kreport.com/methodology