# K143559: XP1000 RF

- Pathway: 510(k) (Traditional)
- Applicant: BTL Industries, Inc.
- Decided: Jun 11, 2015 after 177 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 17 generations back to K943450 (1995). 104 ancestors in all.
7 later devices descend from it; 2 cite it directly.
0 of 112 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120510: Transcend, Syneron Medical, Ltd. (2013) Summary page 4.

## Most influential descendants
- K162512: truSculpt (2016), 5 descendants of its own
- K180709: truSculpt RF Device; truSculpt; truSculpt 3D (2018), 3 descendants of its own
- K172004: truSculpt (2017), 3 descendants of its own
- K221407: truSculpt iD (2022), 2 descendants of its own
- K223110: truSculpt iD (2022), 1 descendant of its own

## Indications for use
The XP1000 RF device is indicated for temporary reduction in circumference of the abdomen.

Source page: https://510kreport.com/device/K143559
Methodology: https://510kreport.com/methodology