Mural Perinatal Surveillance

FDA 510(k) K220732 · Ge Medical Systems Information Technologies, Inc.

Substantially Equivalent

510(k) numberK220732

Submission

Device name
Mural Perinatal Surveillance
Applicant
Ge Medical Systems Information Technologies, Inc.
Wauwatosa, WI, US
Received
March 14, 2022
Decision date
June 23, 2022
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HGM – System, Monitoring, Perinatal
Device class
Class II (moderate risk)
Regulation
21 CFR 884.2740
Specialty
Obstetrics/Gynecology

Other 510(k)s with product code HGM

510(k)DeviceApplicantDecision
K254036Novii+ Wireless Patch SystemHGM · Traditional Datex Ohmeda, Inc.08/10/2026SE
K253021ANNE MaternalHGM · Traditional Sibel Health, Inc.02/26/2026SE
K250777Sonicaid Team3HGM · Traditional Huntleigh Healthcare , Ltd.09/19/2025SE
K241882Fetal & Maternal Monitor (F15A, F15A Air)HGM · Traditional Edan Instruments, Inc.08/27/2025SE
K241368Sonicaid Team3HGM · Traditional Huntleigh Healthcare , Ltd.02/03/2025SE
K241009PeriCALM Patterns 3.0HGM · Traditional Perigen, Inc.01/10/2025SE
K233440Avalon CL Fetal & Maternal (F&M) Pod (866488), Avalon CL Fetal & Maternal (F&M) Patch…HGM · Traditional Philips Medizin Systeme Boeblingen GmbH07/02/2024SE
K231964Novii+ Wireless Patch SystemHGM · Traditional Datex Ohmeda12/08/2023SE
K222327Bloomlife MFM-ProHGM · Traditional Bloom Technologies NV02/13/2023SE
K200975Sonicaid Team3 Antepartum, Sonicaid Team3 IntrapartumHGM · Traditional Huntleigh Healthcare Limited06/24/2020SE

More from Huntleigh Healthcare Limited

510(k)DeviceDecision
K253277Monitor B105M; Monitor B125M; Monitor B155M; Monitor B105P; Monitor B125PMHX · Traditional 07/24/2026SE
K251670MAC 7 Resting ECG Analysis SystemDPS · Traditional 01/26/2026SE
K242562Monitor B105M; Monitor B125M; Monitor B155M; Monitor B105P; Monitor B125PMHX · Traditional 07/09/2025SE
K243540Mac-Lab (AltiX AI.i); CardioLab (AltiX AI.i); ComboLab (AltiX AI.i); MLCL Client…DQK · Special 12/12/2024SE
K233810Portrait VSMMWI · Traditional 04/25/2024SE
K234130Portrait™ Mobile Monitoring Solution consists of: • Portrait™ Central Viewer Application…MWI · Traditional 03/20/2024SE
K231870CASE V7.0 Cardiac Testing System and CardioSoft V7.0 Cardiac Testing SystemDQK · Traditional 12/13/2023SE
K230626Portrait™ Central Viewer Application (Portrait CV A01), Portrait ™ Core Services…MWI · Traditional 08/11/2023SE
K230145One-CufDXQ · Traditional 03/14/2023SE
K222586Mural Clinical ViewerMHX · Traditional 12/21/2022SE

Questions and answers

When was Mural Perinatal Surveillance cleared by the FDA?

Mural Perinatal Surveillance (K220732) received a 510(k) decision of Substantially Equivalent on June 23, 2022, 101 days after the submission was received.

What is the product code of K220732?

The FDA product code is HGM – System, Monitoring, Perinatal, a Class II (moderate risk) device regulated under 21 CFR 884.2740.