# K031881: Airbrush Liposculptor System

- Pathway: 510(k) (Traditional)
- Applicant: Biosculpture Technology, Inc.
- Decided: Jul 28, 2003 after 40 days
- Product code: QPB (System, Suction, Lipoplasty For Removal)
- Device class: 2
- Regulation: 21 CFR 878.5040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Indications for use
The Airbrush T'Liposculptor System is intended to be used for the removal of soft tissue and fluid from the body during general surgical procedures including suction lipoplasty for aesthetic body contouring.

Source page: https://510kreport.com/device/K031881
Methodology: https://510kreport.com/methodology
