FDA 510(k)

SURECELL Gelling Fiber Wound Dressing

K-번호: K173005 · 2018-05-25

신청자Jiangsu Newvalue Medical Producst Co.,Ltd

결정일2018-05-25

제품 코드KGN

결정Substantially Equivalent

기기 요약

SURECELL Gelling Fiber Wound Dressing is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Newvalue Medical Producst Co.,Ltd. It received FDA 510(k) clearance on 2018-05-25 under 510(k) number K173005. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the SURECELL Gelling Fiber Wound Dressing?

SURECELL Gelling Fiber Wound Dressing is a medical device that received FDA 510(k) clearance on 2018-05-25. The listed applicant is Jiangsu Newvalue Medical Producst Co.,Ltd. The 510(k) number is K173005.

When did SURECELL Gelling Fiber Wound Dressing receive FDA 510(k) clearance?

SURECELL Gelling Fiber Wound Dressing received FDA 510(k) clearance on 2018-05-25, under 510(k) number K173005.

Who is the listed applicant for SURECELL Gelling Fiber Wound Dressing?

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

What is the FDA product code for SURECELL Gelling Fiber Wound Dressing?

The FDA product code for SURECELL Gelling Fiber Wound Dressing is KGN.

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SURECELL Gelling Fiber Wound Dressing

기기 요약

자주 묻는 질문

관련 임상시험

관련 기기 (코드: KGN)

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