# K942264: DDR with Dpa and 30/60 Options (Digital Viewstation)

- Pathway: 510(k) (Traditional)
- Applicant: Eigen Video
- Decided: Jul 20, 1994 after 72 days
- Product code: JAA (System, X-Ray, Fluoroscopic, Image-Intensified)
- Device class: 2
- Regulation: 21 CFR 892.1650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K964274: Writestar, and Viewstar (1997), 6 descendants of its own
- K974679: The TCS-Medcon's Telecardiology System (1998), 4 descendants of its own
- K112720: Mckesson Horizon Cardiology (2012), 3 descendants of its own
- K151850: McKesson Cardiology (2015), 2 descendants of its own
- K181080: McKesson Cardiology (2018), 1 descendant of its own

Source page: https://510kreport.com/device/K942264
Methodology: https://510kreport.com/methodology