FDA 510(k)

DR Safety Syringe, Sterile Hypodermic needle for Single use

K-번호: K212226 · 2021-09-29

신청자Zhuhai DR Medical Instruments Co., Ltd.

결정일2021-09-29

제품 코드MEG

자문 위원회HO

결정Substantially Equivalent

기기 요약

DR Safety Syringe, Sterile Hypodermic needle for Single use 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 2021-09-29 under 510(k) number K212226. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the DR Safety Syringe, Sterile Hypodermic needle for Single use?

DR Safety Syringe, Sterile Hypodermic needle for Single use is a medical device that received FDA 510(k) clearance on 2021-09-29. The listed applicant is Zhuhai DR Medical Instruments Co., Ltd.. The 510(k) number is K212226.

When did DR Safety Syringe, Sterile Hypodermic needle for Single use receive FDA 510(k) clearance?

DR Safety Syringe, Sterile Hypodermic needle for Single use received FDA 510(k) clearance on 2021-09-29, under 510(k) number K212226.

Who is the listed applicant for DR Safety Syringe, Sterile Hypodermic needle for Single use?

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 DR Safety Syringe, Sterile Hypodermic needle for Single use?

The FDA product code for DR Safety Syringe, Sterile Hypodermic needle for Single use is MEG.

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

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