# K142048: Emprint Procedure Planning Application

- Pathway: 510(k) (Traditional)
- Applicant: Covidien, LLC
- Decided: Sep 17, 2014 after 51 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K954678 (1996). 20 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 24 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051528: Mevis Liveranalyser/Liverviewer Software, Mevis Technology GmbH & Co. KG (2005) Summary page 4.
- K140093: TABLE, Anatomage, Inc. (2014) Summary page 4.

## Most influential descendants
- K180192: Emprint Ablation Visualization Application (2018), 2 descendants of its own
- K192038: Emprint Visualization Application (2019), 1 descendant of its own
- K252947: HistoSonics® Planning Tool (2026), 0 descendants of its own

## Indications for use
The Emprint™ Procedure Planning Application is a stand-alone software product that allows physicians to visualize and compare CT imaging data. The display, annotation, and volume rendering of medical images aids intervention planning for video-assisted thoracoscopic surgery (VATS) and ablation procedures using the Emprint Ablation System. The software is not intended for diagnosis.

Source page: https://510kreport.com/device/K142048
Methodology: https://510kreport.com/methodology