# K093092: Odyssey Workstation

- Pathway: 510(k) (Special)
- Applicant: Stereotaxis, Inc.
- Decided: Jan 21, 2010 after 112 days
- Product code: DQK (Computer, Diagnostic, Programmable)
- Device class: 2
- Regulation: 21 CFR 870.1425
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Navigant NWS: named in the summary without a submission number

## Most influential descendants
- K253473: Synchrony (2026), 0 descendants of its own

## Indications for use
The Odyssey Workstation is an optional display and user interface package designed to consolidate the point of control of the Catheterization Lab.

Source page: https://510kreport.com/device/K093092
Methodology: https://510kreport.com/methodology