# K150826: Nutra Face Lift Model PE8050

- Pathway: 510(k) (Traditional)
- Applicant: Nutra Luxe MD, LLC
- Decided: Feb 10, 2016 after 317 days
- Product code: NFO (Stimulator, Transcutaneous Electrical, Aesthetic Purposes)
- Device class: 2
- Regulation: 21 CFR 882.5890
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K011935 (2001). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072260: Nuface, Model NU-4003, Carol Cole Company (2007) Summary page 4.

## Indications for use
The Nutra Face LIFT Model PE8050 device is intended for facial stimulation and indicated for over-the-counter cosmetic use.

Source page: https://510kreport.com/device/K150826
Methodology: https://510kreport.com/methodology