# K001336: DR9000 Digital Radiography X-Ray System

- Pathway: 510(k) (Traditional)
- Applicant: Analogic Corp.
- Decided: Jun 2, 2000 after 36 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
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K033345: AN5150 and AN7150 Digital Radiology Systems (2003), 3 descendants of its own
- K040995: Synerad Multi Digital X-Ray System, Model AN6150 (2004), 2 descendants of its own
- K043025: Synerad Omni, Digital X-Ray System, Model AN6250 (2004), 1 descendant of its own
- K071430: Synerad Omni, Models AN6255 and AN6265 (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K001336
Methodology: https://510kreport.com/methodology