# K070079: X3C Digital Radiographic Detector

- Pathway: 510(k) (Special)
- Applicant: Imaging Dynamics Company, Ltd.
- Decided: Jan 31, 2007 after 22 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
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Xaminer: named in the summary without a submission number

## Most influential descendants
- K170202: Aquarius 8600 (2017), 4 descendants of its own
- K181565: Aquarius 8600 Digital Radiography Sensor (2018), 0 descendants of its own
- K173273: Aquarius 8600 1417WCI; Aquarius 8600 1717WCI (2017), 0 descendants of its own
- K171169: Aquarius 8600 1417TG and Aquarius 8600 1717TG (2017), 0 descendants of its own
- K171175: Aquarius 8600 1417WC (2017), 0 descendants of its own

## Indications for use
The X3C (510k submission device) is integrated into the user's stationary radiography system. This typical configuration permits a qualifieditrained doctor or technologist to take a range of head-to-foe diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and other body parts on both adult and pediatric patients. Applications can be performed with patient sitting, standing or lying in the prone or supine positions in an integrated system. The X3C (510k submission device) is nol intended for mammography.

Source page: https://510kreport.com/device/K070079
Methodology: https://510kreport.com/methodology