# K010311: Lipomatic; Lipomatic Liposuction Device

- Pathway: 510(k) (Traditional)
- Applicant: Euromi S.A
- Decided: Jun 29, 2001 after 148 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
Longest line of descent: 1 generation back to K981922 (1998). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K981922: Light Duty Pneumatic Instrument Model Number Pad-100, Heavy Duty Pneumatic Instrument Model Pad-200, Light Duty Electri, Microaire Surgical Instruments, Inc. (1998) Summary page 5.
- K001803: Accelerator Reciprocating Cannula, Byron Medical (2000) Summary page 5.

## Most influential descendants
- K241835: AirSculpt Body Contouring System (AIRS-1-SYS) (2024), 0 descendants of its own

## Indications for use
The subject device is intended to be used for the removal of soft tissue and fluid from the body during general surgical procedures including suction tipoplasty for aesthetic body contouring.

Source page: https://510kreport.com/device/K010311
Methodology: https://510kreport.com/methodology