FDA 510(k)

Curos ジェット滅菌キャップ

K番号: K200299 · 2020-10-29

決定日2020-10-29

製品コードQBP

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

Curos Jet Disinfecting Cap is the device name listed in this FDA 510(k) record. The listed applicant is 3M Company. It received FDA 510(k) clearance on 2020-10-29 under 510(k) number K200299. The device is classified under product code QBP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Curos Jet Disinfecting Cap?

Curos Jet Disinfecting Cap is a medical device that received FDA 510(k) clearance on 2020-10-29. The listed applicant is 3M Company. The 510(k) number is K200299.

When did Curos Jet Disinfecting Cap receive FDA 510(k) clearance?

Curos Jet Disinfecting Cap received FDA 510(k) clearance on 2020-10-29, under 510(k) number K200299.

Who is the listed applicant for Curos Jet Disinfecting Cap?

The FDA 510(k) record lists 3M Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Curos Jet Disinfecting Cap?

The FDA product code for Curos Jet Disinfecting Cap is QBP.

申請者として3M Companyを記載するその他の記録

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