# K063781: Philips XD-S Direct Radiography Workstation/Package

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems North America Co.
- Decided: Jan 5, 2007 after 15 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K915237 (1992). 7 ancestors in all.
16 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)
- K982795: Philips Bucky Vision, Philips Medical Systems, Inc. (1998) Summary page 2.
- K964124: Philips Computed Radiography, Philips Medical Systems, Inc. (1996) Summary page 2.

## Most influential descendants
- K140771: Philips Eleva Workspot (2014), 15 descendants of its own
- K141736: Philips Prograde; Philips Eleva Workspot for Digital Diagnost (2014), 6 descendants of its own
- K203188: ADD (2021), 3 descendants of its own
- K182973: DigitalDiagnost C90 (2019), 3 descendants of its own
- K213497: ADD (Model Name: HAD1417MCW), ADD (Model Name: HAD1717MCW) (2021), 2 descendants of its own

## Recalls of this device
- Jul 9, 2008 · Not classified · Z-2194-2010: Potential for bright artifacts to appear on the patient image from a previous exposure.

## Indications for use
As a part of a radiographic system, the PhilipsXD-S is intended to acquire, process, store, display, and export digital radiographic images. The Philips XD-S is suitable for all routine radiography exams, including specialist areas like intensive care, trauma, or pediatric work, excluding mammography.

Source page: https://510kreport.com/device/K063781
Methodology: https://510kreport.com/methodology