Current Health System

FDA 510(k) K222550 · Current Health , Ltd.

Substantially Equivalent

510(k) numberK222550

Submission

Device name
Current Health System
Applicant
Current Health , Ltd.
Edinburgh, GB
Received
August 23, 2022
Decision date
November 1, 2022
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MSX – System, Network And Communication, Physiological Monitors
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2300
Specialty
Cardiovascular
Life-sustaining
Yes

Other 510(k)s with product code MSX

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K261287Digistat CareMSX · Traditional Ascom Ums Srl Unipersonale09/12/2026SE
K260211Dashboard (P007000)MSX · Traditional Hill-Rom, Inc.08/13/2026SE
K261367Corsano CardioWatch 287-2 SystemMSX · Traditional Corsano Health B.V.07/26/2026SE
K253654IntelliVue Measurement Rack 6000 (867317)MSX · Traditional Philips Medizin Systeme Böblingen GmbH03/30/2026SE
K243270TigerConnect Alarm ManagementMSX · Traditional Tigerconnect09/30/2025SE
K242728BeneVision Central Monitoring SystemMSX · Traditional Shenzhen Mindray Bio-Medical Electronics Co., Ltd.07/31/2025SE
K242750Central StationMSX · Traditional Nihon Kohden Digital Health Solutions, LLC06/05/2025SE
K242842ANNE View, Central HubMSX · Traditional Sibel Health, Inc.01/08/2025SE
K241397HinscopeMSX · Traditional Hinlab Sas11/14/2024SE
K233834Infinity Gateway SuiteMSX · Traditional Draeger Medical Systems, Inc.07/12/2024SE

More from Draeger Medical Systems, Inc.

510(k)DeviceDecision
K231506Current Health SystemMSX · Special 08/24/2023SE
K210133Current Health Monitoring System Gen 2 (G2)MSX · Traditional 09/03/2021SE
K191272Wearable Device, Wearable PackageMSX · Traditional 07/12/2019SE
K190073Wearable Device, Home Package in Carry Case with Homehub, Home Package in Carry Case…MSX · Traditional 03/27/2019SE

Questions and answers

When was Current Health System cleared by the FDA?

Current Health System (K222550) received a 510(k) decision of Substantially Equivalent on November 1, 2022, 70 days after the submission was received.

What is the product code of K222550?

The FDA product code is MSX – System, Network And Communication, Physiological Monitors, a Class II (moderate risk) device regulated under 21 CFR 870.2300.