FDA 510(k)

Sterile Hypodermic Syringe for Single Use

K-번호: K212207 · 2023-03-23

신청자Shandong Weigao Group Medical Polymer Co., Ltd.

결정일2023-03-23

제품 코드FMF

자문 위원회HO

결정Substantially Equivalent

기기 요약

Sterile Hypodermic Syringe for Single Use is the device name listed in this FDA 510(k) record. The listed applicant is Shandong Weigao Group Medical Polymer Co., Ltd.. It received FDA 510(k) clearance on 2023-03-23 under 510(k) number K212207. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the Sterile Hypodermic Syringe for Single Use?

Sterile Hypodermic Syringe for Single Use is a medical device that received FDA 510(k) clearance on 2023-03-23. The listed applicant is Shandong Weigao Group Medical Polymer Co., Ltd.. The 510(k) number is K212207.

When did Sterile Hypodermic Syringe for Single Use receive FDA 510(k) clearance?

Sterile Hypodermic Syringe for Single Use received FDA 510(k) clearance on 2023-03-23, under 510(k) number K212207.

Who is the listed applicant for Sterile Hypodermic Syringe for Single Use?

The FDA 510(k) record lists Shandong Weigao Group Medical Polymer Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sterile Hypodermic Syringe for Single Use?

The FDA product code for Sterile Hypodermic Syringe for Single Use is FMF.

Shandong Weigao Group Medical Polymer Co., Ltd.를 신청인으로 등재한 기타 기록

K212920Sterile Safety Syringe with Needle for Single Use, Sterile Safety Hypodermic Needle for Single Use,Sterile Auto-Disable Syringe with Needle for Single Use

공식 출처

FDA 데이터베이스에서 보기 →

FDA Open API에서 수집된 데이터입니다. 가장 정확하고 공인된 정보는 항상 공식 레코드를 참조하시기 바랍니다.