# K040931: Patxfer RT

- Pathway: 510(k) (Traditional)
- Applicant: Brainlab AG
- Decided: Jul 22, 2004 after 104 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: 2 generations back to K983831 (1999). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K021583: Patxfer, Brainlab AG (2002) Summary page 1.

## Indications for use
PatXfer RT provides capabilities for the acceptance, transfer, display, storage, and digital processing of medical images and objects according to the DICOM RT standard and according to the BrainLAB proprietary data format. This includes functions for performing operations related to image manipulation, enhancement, compression, and quantification. The integrity of the original data is maintained.

Source page: https://510kreport.com/device/K040931
Methodology: https://510kreport.com/methodology