# K021583: Patxfer

- Pathway: 510(k) (Traditional)
- Applicant: Brainlab AG
- Decided: Aug 12, 2002 after 90 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: 1 generation back to K983831 (1999). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K983831: VECTORVISION2, Brainlab AG (1999) Summary page 2.
- (no number) VectorVision: named in the summary without a submission number

## Most influential descendants
- K040931: Patxfer RT (2004), 0 descendants of its own

## Indications for use
PatXfer provides capabilities for the acceptance, transfer, display, storage and digital processing of medical images including functions for performing operations related to image manipulation,

Source page: https://510kreport.com/device/K021583
Methodology: https://510kreport.com/methodology