FDA 510(k)

ビニル/ニトリルブレンド検査手袋

K番号: K213634 · 2022-02-18

申請者Dezhou Hengchang Medical Technology Co., Ltd.

決定日2022-02-18

製品コードLYZ

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]

決定大幅同等

医療機器の概要

Vinyl/Nitrile Blend Exam Glove is the device name listed in this FDA 510(k) record. The listed applicant is Dezhou Hengchang Medical Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-02-18 under 510(k) number K213634. The device is classified under product code LYZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Vinyl/Nitrile Blend Exam Glove?

Vinyl/Nitrile Blend Exam Glove is a medical device that received FDA 510(k) clearance on 2022-02-18. The listed applicant is Dezhou Hengchang Medical Technology Co., Ltd.. The 510(k) number is K213634.

When did Vinyl/Nitrile Blend Exam Glove receive FDA 510(k) clearance?

Vinyl/Nitrile Blend Exam Glove received FDA 510(k) clearance on 2022-02-18, under 510(k) number K213634.

Who is the listed applicant for Vinyl/Nitrile Blend Exam Glove?

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

What is the FDA product code for Vinyl/Nitrile Blend Exam Glove?

The FDA product code for Vinyl/Nitrile Blend Exam Glove is LYZ.

申請者としてDezhou Hengchang Medical Technology Co., Ltd.を記載するその他の記録

K220055disposable, ビニル検査手袋, ゆうろ K213625ビニル検査手袋

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