Embrace

FDA 510(k) K172935 · Empatica S.r.l.

Substantially Equivalent

510(k) numberK172935

Submission

Device name
Embrace
Applicant
Empatica S.r.l.
Milano, IT
Received
September 26, 2017
Decision date
January 26, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
POS – Physiological Signal Based Seizure Monitoring System
Device class
Class II (moderate risk)
Regulation
21 CFR 882.1580
Specialty
Neurology

The Physiological signal based seizure monitoring system is a prescription device that uses physiological signal to identify abnormal physiological activity that may be associated with a seizure. The System does not predict seizure onsets, and is not intended as a standalone seizure monitoring device.

Other 510(k)s with product code POS

510(k)DeviceApplicantDecision
K251506Nelli (Version 7.11)POS · Traditional Neuro Event Labs OY11/21/2025SE
K243199NightWatch+ USPOS · Traditional Livassured BV07/12/2025SE
K250515EpiMonitorPOS · Special Empatica S.r.l.06/19/2025SE
K243515EpiWatch Monitoring SystemPOS · Traditional Epiwatch, Inc.03/07/2025SE
K232915EpiMonitorPOS · Traditional Empatica S.r.l.02/15/2024SE
K200276SPEAC SystemPOS · Traditional Brain Sentinel, Inc.02/06/2021SE
K182180SPEAC SystemPOS · Traditional Brain Sentinel, Inc.05/11/2019SE
K181861EmbracePOS · Traditional Empatica S.r.l.12/20/2018SE

More from Empatica S.r.l.

510(k)DeviceDecision
K260374Empatica Health Monitoring Platform for Parkinson's Disease Monitoring; EmbracePlus…GYD · Traditional 08/14/2026SE
K252981EmbraceMiniLEL · Traditional 12/22/2025SE
K250515EpiMonitorPOS · Special 06/19/2025SE
K242737Empatica Health Monitoring Platform; EmbracePlus; Empatica Care; Care PortalMWI · Traditional 06/06/2025SE
K232915EpiMonitorPOS · Traditional 02/15/2024SE
K230457Empatica Health Monitoring Platform; EmbracePlus; Empatica Care; Care PortalMWI · Traditional 10/30/2023SE
K221282Empatica Health Monitoring PlatformDQA · Traditional 11/20/2022SE
K181861EmbracePOS · Traditional 12/20/2018SE

Questions and answers

When was Embrace cleared by the FDA?

Embrace (K172935) received a 510(k) decision of Substantially Equivalent on January 26, 2018, 122 days after the submission was received.

What is the product code of K172935?

The FDA product code is POS – Physiological Signal Based Seizure Monitoring System, a Class II (moderate risk) device regulated under 21 CFR 882.1580.