FDA 510(k)

Extension tube

K-번호: K251788 · 2026-03-05

신청자Zhuhai DR Medical Instruments Co., Ltd.

결정일2026-03-05

제품 코드DXT

자문 위원회CV

결정Substantially Equivalent

기기 요약

Extension tube is the device name listed in this FDA 510(k) record. The listed applicant is Zhuhai DR Medical Instruments Co., Ltd.. It received FDA 510(k) clearance on 2026-03-05 under 510(k) number K251788. The device is classified under product code DXT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Extension tube?

Extension tube is a medical device that received FDA 510(k) clearance on 2026-03-05. The listed applicant is Zhuhai DR Medical Instruments Co., Ltd.. The 510(k) number is K251788.

When did Extension tube receive FDA 510(k) clearance?

Extension tube received FDA 510(k) clearance on 2026-03-05, under 510(k) number K251788.

Who is the listed applicant for Extension tube?

The FDA 510(k) record lists Zhuhai DR Medical Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Extension tube?

The FDA product code for Extension tube is DXT.

Zhuhai DR Medical Instruments Co., Ltd.를 신청인으로 등재한 기타 기록

K212226DR Safety Syringe, Sterile Hypodermic needle for Single use

관련 기기 (코드: DXT)

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