# K912639: Sonicaid Team

- Pathway: 510(k) (Traditional)
- Applicant: Oxford Medilog, Inc.
- Decided: Dec 31, 1991 after 200 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.
29 later devices descend from it; 1 cites it directly.
0 of 30 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K992607: Sonicaid System 8002 (2001), 28 descendants of its own
- K081140: Visensia (2008), 22 descendants of its own
- K110953: Visensia, Visensia with Alert (2011), 17 descendants of its own
- K152258: T3 Software (2016), 16 descendants of its own
- K163065: T3 Software (2017), 15 descendants of its own

Source page: https://510kreport.com/device/K912639
Methodology: https://510kreport.com/methodology