# K894958: Model 410 Alert and Telecommunication System

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems Information Technologies
- Decided: Nov 3, 1989 after 88 days
- Product code: HGM (System, Monitoring, Perinatal)
- Device class: 2
- Regulation: 21 CFR 884.2740
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 1 cites it directly.
0 of 11 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
- K993008: Quantitative Sentinel System (1999), 9 descendants of its own
- K051175: Civ-OB Obstrical Monitoring Software Application (2006), 4 descendants of its own
- K103172: Civ-OB (Plus) (2011), 3 descendants of its own
- K143695: Central Monitoring System (2015), 1 descendant of its own
- K020661: Unity IS Patient Viewer (2002), 1 descendant of its own

Source page: https://510kreport.com/device/K894958
Methodology: https://510kreport.com/methodology