# K992955: Xplorer 1000

- Pathway: 510(k) (Traditional)
- Applicant: Imaging Dynamics Corp.
- Decided: Jun 2, 2000 after 275 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 K974863 (1998). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K974863: Imix Digital Thorax System, Advanced Instrument Development, Inc. (1998) Summary page 1.
- (no number) conventional radiographic film: named in the summary without a submission number

## Most influential descendants
- K093816: Digital Radiography System, Models Galaxy 900 and 1600 (2010), 0 descendants of its own

## Indications for use
Intended for use in general human radiography imaging similar to the optically coupled CCD based device cleared under 510(k) number K974863. Not to be used for mammography.

Source page: https://510kreport.com/device/K992955
Methodology: https://510kreport.com/methodology