FDA 510(k)

Central Station

Номер K: K242750 · 2025-06-05

ЗаявительNihon Kohden Digital Health Solutions, LLC

Дата решения2025-06-05

Код продуктаMSX

Консультативный комитетCV

РешениеSubstantially Equivalent

Описание устройства

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.

Часто задаваемые вопросы

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.

Связанные клинические исследования

Связанные записи сопоставляются автоматически на основании названий, кодов продукции или иных метаданных. Сопоставление не подтверждает клиническую, научную, корпоративную или регуляторную связь; ознакомьтесь с официальными источниками по ссылкам.

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Связанные устройства (Код: MSX)

K261287Digistat CareAscom Ums Srl Unipersonale K260211Dashboard (P007000)Hill-Rom, Inc.K261367Corsano CardioWatch 287-2 SystemCorsano Health B.V.K253654IntelliVue Measurement Rack 6000 (867317)Philips Medizin Systeme Böblingen GmbH K243270TigerConnect Alarm ManagementTigerconnect K242728BeneVision Central Monitoring SystemShenzhen Mindray Bio-Medical Electronics Co., Ltd.

Официальный источник

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