# K253473: Synchrony

- Pathway: 510(k) (Traditional)
- Applicant: Stereotaxis, Inc.
- Decided: Apr 1, 2026 after 173 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
Longest line of descent: 1 generation back to K072371 (2007). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K093092: Odyssey Workstation, Stereotaxis, Inc. (2010) Summary page 5.
- K072371: Odyssey Workstation, Stereotaxis, Inc. (2007) Summary page 5.

## Indications for use
The Stereotaxis Synchrony™ system is an optional display and user interface package designed to consolidate the point of control of a medical lab.

Source page: https://510kreport.com/device/K253473
Methodology: https://510kreport.com/methodology