# P890063: Genesis (R) Home Uterine Activity Monitoring System

- Pathway: PMA
- Applicant: Matria Healthcare, Inc.
- Decided: Sep 12, 1990 after 301 days
- Product code: HFM (Monitor, Uterine Contraction, External (For Use In Clinic))
- Device class: 2
- Regulation: 21 CFR 884.2720
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. PMA decisions do not claim a predicate device.

Source page: https://510kreport.com/device/P890063
Methodology: https://510kreport.com/methodology