FDA 510(k)

SURECELL ガelling ファイバーウォンドデイシング

K番号: K173005 · 2018-05-25

申請者Jiangsu Newvalue Medical Producst Co.,Ltd

決定日2018-05-25

製品コードKGN

決定大幅同等

医療機器の概要

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.

よくある質問

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 ガelling ファイバーウォンドデイシング

医療機器の概要

よくある質問

関連する臨床試験

関連機器（コード：KGN）

公式ソース