# K200545: Legend Pro DMA

- Pathway: 510(k) (Traditional)
- Applicant: Pollogen, Ltd.
- Decided: Oct 21, 2021 after 597 days
- Product code: NGX (Stimulator, Muscle, Powered, For Muscle Conditioning)
- Device class: 2
- Regulation: 21 CFR 890.5850
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K940301 (1994). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K182440: Body System, A-1 Engineering (2019) Summary page 4.

## Most influential descendants
- K233470: Deka Lily (2023), 0 descendants of its own

## Indications for use
Legend Pro DMA is intended for muscle conditioning to stimulate healthy muscles. Legend Pro DMA is not intended to be used in conjunction with therapy or treatment of medical diseases or medical conditions of any kind. Legend Pro DMA is intended to be operated by a trained professional who is present to monitor treatment

Source page: https://510kreport.com/device/K200545
Methodology: https://510kreport.com/methodology