FDA 510(k)

UniTex Non-Sterile, Powder-Free, Latex Examination Glove

K番号: K161961 · 2017-05-11

決定日2017-05-11

製品コードLYY

諮問委員会医療機器規制テキストの翻訳は以下の通りです。 HO [翻訳が提供されなかったため、原文の「HO」がそのまま使用されます]

決定Substantially Equivalent

医療機器の概要

UniTex Non-Sterile, Powder-Free, Latex Examination Glove is the device name listed in this FDA 510(k) record. The listed applicant is Ug Global Resources Sdn. Bhd.. It received FDA 510(k) clearance on 2017-05-11 under 510(k) number K161961. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the UniTex Non-Sterile, Powder-Free, Latex Examination Glove?

UniTex Non-Sterile, Powder-Free, Latex Examination Glove is a medical device that received FDA 510(k) clearance on 2017-05-11. The listed applicant is Ug Global Resources Sdn. Bhd.. The 510(k) number is K161961.

When did UniTex Non-Sterile, Powder-Free, Latex Examination Glove receive FDA 510(k) clearance?

UniTex Non-Sterile, Powder-Free, Latex Examination Glove received FDA 510(k) clearance on 2017-05-11, under 510(k) number K161961.

Who is the listed applicant for UniTex Non-Sterile, Powder-Free, Latex Examination Glove?

The FDA 510(k) record lists Ug Global Resources Sdn. Bhd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UniTex Non-Sterile, Powder-Free, Latex Examination Glove?

The FDA product code for UniTex Non-Sterile, Powder-Free, Latex Examination Glove is LYY.

申請者としてUg Global Resources Sdn. Bhd.を記載するその他の記録

K232319ブラックパールニトリル検査手袋 K162510非滅菌、粉体不使用、ニトリル検査手袋、青色

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