# K870692: Perinatal Computers 2015/2025/2040/2045/2080/2085

- Pathway: 510(k) (Traditional)
- Applicant: Peritronics Research and Development, Inc.
- Decided: May 4, 1987 after 74 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.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K974248: Watchchild Obsterical Patient Data Management System (1998), 2 descendants of its own
- K014094: Modification to the Watchchild Obstetrical Patient Data Management System (2002), 1 descendant of its own
- K032772: Modification to Watchchild Obstetrical Patient Data Management System (Also Referred to as) the Watchchild System (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K870692
Methodology: https://510kreport.com/methodology