# K233470: Deka Lily

- Pathway: 510(k) (Traditional)
- Applicant: El.En S.P.A.
- Decided: Dec 19, 2023 after 55 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: 7 generations back to K940301 (1994). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K200545: Legend Pro DMA, Pollogen, Ltd. (2021) Summary page 6.

## Indications for use
The LILY device is indicated for muscle conditioning to stimulate healty muscles. The device is not intended to be used in conjunction with therapy or treatment of medical disease or medical conditions of any kind. The device is intended to be operated by a trained professional who is present to monitor treatment.

Source page: https://510kreport.com/device/K233470
Methodology: https://510kreport.com/methodology