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FDA 510(k)

Central Station

K-Number: K242750 · 2025-06-05

ApplicantNihon Kohden Digital Health Solutions, LLC
Decision Date2025-06-05
Product CodeMSX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Central Station is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden Digital Health Solutions, LLC. It received FDA 510(k) clearance on 2025-06-05 under 510(k) 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. The listed applicant is Nihon Kohden Digital Health Solutions, LLC. The 510(k) number is K242750.

When did Central Station receive FDA 510(k) clearance?

Central Station received FDA 510(k) clearance on 2025-06-05, under 510(k) number K242750.

Who is the listed applicant for Central Station?

The FDA 510(k) record lists Nihon Kohden Digital Health Solutions, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Central Station?

The FDA product code for Central Station is MSX.

Other records listing Nihon Kohden Digital Health Solutions, LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K220989Next Generation NetKonnect

Related Devices (Code: MSX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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