# K073632: Intuition, Model 0170

- Pathway: 510(k) (Traditional)
- Applicant: Arcoma AB
- Decided: Jan 10, 2008 after 15 days
- Product code: KPR (System, X-Ray, Stationary)
- 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: 2 generations back to K042041 (2004). 4 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011486: Q-Rad Radiographic System, Quantum Medical Imaging, LLC (2001) Summary page 1.
- K063039: Xplorer 2200 Digital Radiographic System, Imaging Dynamics Company, Ltd. (2006) Summary page 1.
- K050925: Digital Radiography System Radspeed Safire, Shimadzu Corp. (2005) Summary page 1.

## Most influential descendants
- K140683: 0180 Intuition, 0072 Precision (2014), 0 descendants of its own
- K121109: Aerodr X70 (2012), 0 descendants of its own

## Indications for use
The 0170 Intuition is a stationery x-ray system intended for obtaining radiographic images of various portions of the human body in a clinical environment. The 0170 Intuition is not intended for mammography

Source page: https://510kreport.com/device/K073632
Methodology: https://510kreport.com/methodology