# K220732: Mural Perinatal Surveillance

- Pathway: 510(k) (Traditional)
- Applicant: Ge Medical Systems Information Technologies, Inc.
- Decided: Jun 23, 2022 after 101 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
Longest line of descent: 23 generations back to K941811 (1994). 130 ancestors in all.
No later device cites it as a predicate yet.
0 of 131 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K173941: IntelliSpace Perinatal Rev.K.00, Philips Medizin Systeme Boeblingen GmbH (2018) Summary page 4.

## Indications for use
Mural Perinatal Surveillance is a perinatal monitoring system intended for electronic collection, display, and documentation of clinical data with optional features to store, export, annotate, calculate, and retrieve clinical data. Data is acquired from medical devices, electronic health records, or other data sources on a hospital’s network. This device is intended for use by healthcare professionals in clinical support settings for obstetric patients during and after pregnancy. This product is not intended to control or alter any of the medical devices providing data across the hospital network. All information or indications provided are intended to support the judgment of medical professionals and are not intended to be the sole source of information for decision making.

Source page: https://510kreport.com/device/K220732
Methodology: https://510kreport.com/methodology