FDA 510(k)

DEKA Infusion System, DEKA Administration Set

Номер K: K242693 · 2024-10-07

ЗаявительDeka Research and Development Corporation

Дата решения2024-10-07

Код продуктаLDR

Консультативный комитетHO

РешениеSubstantially Equivalent

Описание устройства

DEKA Infusion System, DEKA Administration Set is the device name listed in this FDA 510(k) record. The listed applicant is Deka Research and Development Corporation. It received FDA 510(k) clearance on 2024-10-07 under 510(k) number K242693. The device is classified under product code LDR. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Часто задаваемые вопросы

What is the DEKA Infusion System, DEKA Administration Set?

DEKA Infusion System, DEKA Administration Set is a medical device that received FDA 510(k) clearance on 2024-10-07. The listed applicant is Deka Research and Development Corporation. The 510(k) number is K242693.

When did DEKA Infusion System, DEKA Administration Set receive FDA 510(k) clearance?

DEKA Infusion System, DEKA Administration Set received FDA 510(k) clearance on 2024-10-07, under 510(k) number K242693.

Who is the listed applicant for DEKA Infusion System, DEKA Administration Set?

The FDA 510(k) record lists Deka Research and Development Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEKA Infusion System, DEKA Administration Set?

The FDA product code for DEKA Infusion System, DEKA Administration Set is LDR.

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: LDR)

K232316DEKA Infusion System, DEKA Administration SetDeka Research and Development K153760Volumetric Infusion ControllerDEKA Research & Development

Официальный источник

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