# K962010: Epi-Scope Option for Q Series CT Systems

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems (Cleveland), Inc.
- Decided: Mar 21, 1997 after 302 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- 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 K954355 (1995). 1 ancestor in all.
9 later devices descend from it; 2 cite it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K954355: Advantage Windows 3D with Navigator Option, General Electric Co. (1995) Summary page 1.

## Most influential descendants
- K990241: Accuimage, Accuview Diagnostic Imaging, Workstation W/Accuscore, Accuanalyze, Accuscope, Accushade, Accuvrt, and Accumip (1999), 8 descendants of its own
- K063221: Medweb Advanced 3D Web Pacs (2006), 1 descendant of its own
- K024149: Primelung (2003), 1 descendant of its own
- K082336: XR-Express (2008), 0 descendants of its own
- K070868: LMS-Lung/Track (2007), 0 descendants of its own

## Indications for use
The epi-Scope Option will be used in a Computed Tomography X-ray System intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from the same axial plane taken at different angles. This device may include signal analysis and display equipment, patient equipment supports, components and accessories.

Source page: https://510kreport.com/device/K962010
Methodology: https://510kreport.com/methodology