# K151722: Slim UP ULTRA

- Pathway: 510(k) (Traditional)
- Applicant: Aime Medical, Inc.
- Decided: Mar 18, 2016 after 267 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 K010335 (2001). 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)
- K123075: Buttock Muscle Stimulator Model WL-2413B; Buttock Muscle Stimulator Mode WL-2413E, Well-Life Healthcare Limited (2013) Summary page 5.

## Indications for use
Slim UP® ULTRA is indicated for the use by healthy persons to apply transcutaneous electrical muscle stimulation (EMS) through skin contact electrode for the purpose of improvement of muscle tone of buttocks muscles.

Source page: https://510kreport.com/device/K151722
Methodology: https://510kreport.com/methodology