FDA 510(k)

DEKA Infusion System, DEKA Administration Set

Número K: K242693 · 2024-10-07

RequerenteDeka Research and Development Corporation

Data da decisão2024-10-07

Código do produtoLDR

Comité consultivoHO

DecisãoSubstantially Equivalent

Resumo do dispositivo

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.

Perguntas frequentes

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.

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Dispositivos Relacionados (Código: LDR)

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

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