# K170202: Aquarius 8600

- Pathway: 510(k) (Special)
- Applicant: Imaging Dynamics Company, Ltd.
- Decided: Feb 22, 2017 after 30 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: 1 generation back to K070079 (2007). 1 ancestor in all.
4 later devices descend from it; 4 cite 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)
- K070079: X3C Digital Radiographic Detector, Imaging Dynamics Company, Ltd. (2007) Summary page 4.

## Most influential descendants
- 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
Intended for use by a qualified/trained doctor or technologist on both adult and pediatric patients for taking 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. Not intended for mammography.

Source page: https://510kreport.com/device/K170202
Methodology: https://510kreport.com/methodology