FDA 510(k)

DEKA Infusion System, DEKA Administration Set

K-번호: K242693 · 2024-10-07

신청자Deka Research and Development Corporation

결정일2024-10-07

제품 코드LDR

자문 위원회HO

결정Substantially Equivalent

기기 요약

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.

자주 묻는 질문

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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DEKA Infusion System, DEKA Administration Set

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관련 임상시험

관련 기기 (코드: LDR)

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