# K152731: XP1100 RF

- Pathway: 510(k) (Traditional)
- Applicant: BTL Industries, Inc.
- Decided: Jul 20, 2016 after 302 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: 18 generations back to K943450 (1995). 105 ancestors in all.
No later device cites it as a predicate yet.
0 of 106 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K143559: XP1000 RF, BTL Industries, Inc. (2015) Summary page 4.

## Indications for use
The XP1100 RF is indicated for temporary reduction in circumference of the abdomen and thighs.

Source page: https://510kreport.com/device/K152731
Methodology: https://510kreport.com/methodology