# K870039: Imagenet Digital Ophthalmic Imaging System

- Pathway: 510(k) (Traditional)
- Applicant: Par Microsystems Corp.
- Decided: Feb 12, 1987 after 38 days
- Product code: DSF (Recorder, Paper Chart)
- Device class: 1
- Regulation: 21 CFR 870.2810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
56 later devices descend from it; 5 cite it directly.
0 of 57 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
- K082364: Imagenet Professional PC Software System or Imagenet Professional, or Imagenet Pro, or Digital Imaging Software for (2008), 50 descendants of its own
- K093313: Synergy (2009), 29 descendants of its own
- K122938: Forum Forum Archive Forum Archive & Viewer Forum Assist Match (2012), 25 descendants of its own
- K101861: Truevision 3D Visualization and Guidance System (2010), 13 descendants of its own
- K132667: Synergy Odm (2013), 9 descendants of its own

Source page: https://510kreport.com/device/K870039
Methodology: https://510kreport.com/methodology