Central Station
K-Number: K242750 · 2025-06-05
Decision Date2025-06-05
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Central Station is a medical device manufactured by Nihon Kohden Digital Health Solutions, LLC. It received FDA 510(k) clearance on 2025-06-05 under approval number K242750. The device is classified under product code MSX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Central Station?
Central Station is a medical device that received FDA 510(k) clearance on 2025-06-05. It is manufactured by Nihon Kohden Digital Health Solutions, LLC. The 510(k) number is K242750.
When was Central Station approved by the FDA?
Central Station received FDA 510(k) clearance on 2025-06-05, under approval number K242750.
What company makes Central Station?
Central Station is manufactured by Nihon Kohden Digital Health Solutions, LLC.
What is the FDA product code for Central Station?
The FDA product code for Central Station is MSX.
Related Clinical Trials
Related Devices (Code: MSX)
K153156eCareManager 4.0.1Visicu, Inc.
K160862AirStrip RPMAirstrip Technologies, Inc.
K161164CareEvent inclusive of the CareEvent Mobile Application accessoryPhilips Medical Systems
K171322eCareManager 4.1Visicu, Inc.
K162607BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd.
K180430Digistat Smart CentralAscom Ums Srl Unipersonale
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.