# K071682: Crystalview T-Series Computed Radiography System, Models T110 (with Eraser) and T100 (Without Eraser)

- Pathway: 510(k) (Traditional)
- Applicant: Alara, Inc.
- Decided: Aug 15, 2007 after 57 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: 2 generations back to K884621 (1989). 7 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042023: Fuji Computed Radiography (FCR) Clearview CS Image Reader, Fujifilm Medical System U.S.A., Inc. (2004) Summary page 1.
- K955643: Alara Imaging System, Denoptix, Inc. (1996) Summary page 1.

## Most influential descendants
- K102479: Alara T210 Computed Radiography System (2011), 0 descendants of its own

## Indications for use
The CRystalView T-Series is indicated for use in generating radiographic images of human anatomy. It is intended to replace radiographic film/screen systems in general-purpose diagnostic procedures. The CRystalView T-Series is not indicated for use in mammography.

Source page: https://510kreport.com/device/K071682
Methodology: https://510kreport.com/methodology