# K934959: Model 118 Fetal/Maternal Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems Information Technologies
- Decided: Aug 15, 1994 after 304 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.
25 later devices descend from it; 4 cite it directly.
0 of 26 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
- K964770: Corometrics 120 Series Maternal/Fetal Monitor (1997), 16 descendants of its own
- K991739: Corometrics 120 Series Maternal/Fetal Monitor (1999), 10 descendants of its own
- K082602: Fetal & Maternal Monitor, Model F6, F9 (2008), 6 descendants of its own
- K994008: Biosys Fetal Monitor, Model Ifm-500 (2000), 6 descendants of its own
- K100797: Fetal Maternal Monitor Model F9 Express and Express (2010), 5 descendants of its own

Source page: https://510kreport.com/device/K934959
Methodology: https://510kreport.com/methodology