# K992698: Stentor, Pageview

- Pathway: 510(k) (Traditional)
- Applicant: Stentor, Inc.
- Decided: Oct 25, 1999 after 75 days
- Product code: LMD (System, Digital Image Communications, Radiological)
- Device class: 1
- Regulation: 21 CFR 892.2020
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K954678 (1996). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K982769: Mitra Imaging Inc. Exhibit, Mitra Imaging, Inc. (1998) Summary page 2.
- K983815: Pacscache, Dome Imaging Systems, Inc. (1999) Summary page 2.

## Indications for use
Stentor PageView is a digital medical imaging distribution and display system to be used for both primary diagnosis and efficient distribution of medical images within the healthcare enterprise. It operates on the conventional TCP/IP internetworking infrastructure available in most healthcare organizations, and it uses commercially available computer platforms (Intel Pentium-based) and operating systems (Microsoft Windows NT, Windows 95, and Windows 98). The system does not permanently store or produce original medical images.

Source page: https://510kreport.com/device/K992698
Methodology: https://510kreport.com/methodology