# K071573: Rugalift, Model# V.2.1

- Pathway: 510(k) (Abbreviated)
- Applicant: Fatrotek S.R.L.
- Decided: Dec 9, 2008 after 550 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: 1 generation back to K011935 (2001). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011935: Rejuvenique Model #RJV10, Salton, Inc. (2001) Summary page 1.

## Most influential descendants
- K102494: The Buzz Facial Toning System (2011), 0 descendants of its own

## Indications for use
The RUGALIFT is indicated for cosmetic use.

Source page: https://510kreport.com/device/K071573
Methodology: https://510kreport.com/methodology