# K182973: DigitalDiagnost C90

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems Dmc GmbH
- Decided: Jan 11, 2019 after 77 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: 9 generations back to K803130 (1981). 29 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141736: Philips Prograde; Philips Eleva Workspot for Digital Diagnost, Philips Medical Systems Dmc GmbH (2014) Summary page 4.
- K982795: Philips Bucky Vision, Philips Medical Systems, Inc. (1998) Summary page 5.

## Most influential descendants
- K202564: DigitalDiagnost C90 (2020), 2 descendants of its own
- K210692: DigitalDiagnost (2021), 1 descendant of its own
- K212186: Philips Radiology Smart Assistant (2021), 0 descendants of its own

## Indications for use
The DigitalDiagnost C90 is intended to acquire, process, store, display and export digital radiographic images. The DigitalDiagnost C90 is suitable for all routine radiography examinations, including specialist areas like intensive care, trauma or pediatric work, excluding fluoroscopy, angiography and mammography.

Source page: https://510kreport.com/device/K182973
Methodology: https://510kreport.com/methodology