# K213097: Armory Motion

- Pathway: 510(k) (Traditional)
- Applicant: Pain Management Technologies, Inc.
- Decided: Jun 10, 2022 after 259 days
- Product code: ILO (Pack, Hot Or Cold, Water Circulating)
- Device class: 2
- Regulation: 21 CFR 890.5720
- 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 K944567 (1995). 14 ancestors in all.
No later device cites it as a predicate yet.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183702: Polar Care Wave, Breg, Inc. (2019) Summary page 4.

## Indications for use
The Armory Motion is a prescription device that combines cold and compression therapy and is intended to treat post-surgical and acute injuries to reduce edema, swelling, and pain for which cold and compression are indicated. Armory Motion is intended to be used by a licensed health care professional in rehabilitation facilities, outpatient clinics, athletic training settings, and home settings.

Source page: https://510kreport.com/device/K213097
Methodology: https://510kreport.com/methodology