# K140771: Philips Eleva Workspot

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems Dmc GmbH
- Decided: Apr 25, 2014 after 29 days
- Product code: MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager))
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K803130 (1981). 26 ancestors in all.
15 later devices descend from it; 4 cite it directly.
0 of 42 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063781: Philips XD-S Direct Radiography Workstation/Package, Philips Medical Systems North America Co. (2007) Summary page 1.
- K122736: DX-D Imaging Package, Agfa Healthcare N.V. (2013) Summary page 2.

## Most influential descendants
- 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
- K202564: DigitalDiagnost C90 (2020), 2 descendants of its own

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

Source page: https://510kreport.com/device/K140771
Methodology: https://510kreport.com/methodology