FDA 510(k)

医療用フェイスマスク、モデル名：MY020003

K番号: K211165 · 2021-11-09

申請者Huizhou Jie Bai Purification Co., Ltd.

決定日2021-11-09

製品コードFXX

諮問委員会SU （以下のテキストは翻訳されていません。） Policy: medical-regulatory-v1

決定大幅同等

医療機器の概要

Medical Face Masks, Model Name:MY020003 is the device name listed in this FDA 510(k) record. The listed applicant is Huizhou Jie Bai Purification Co., Ltd.. It received FDA 510(k) clearance on 2021-11-09 under 510(k) number K211165. The device is classified under product code FXX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Medical Face Masks, Model Name:MY020003?

Medical Face Masks, Model Name:MY020003 is a medical device that received FDA 510(k) clearance on 2021-11-09. The listed applicant is Huizhou Jie Bai Purification Co., Ltd.. The 510(k) number is K211165.

When did Medical Face Masks, Model Name:MY020003 receive FDA 510(k) clearance?

Medical Face Masks, Model Name:MY020003 received FDA 510(k) clearance on 2021-11-09, under 510(k) number K211165.

Who is the listed applicant for Medical Face Masks, Model Name:MY020003?

The FDA 510(k) record lists Huizhou Jie Bai Purification Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medical Face Masks, Model Name:MY020003?

The FDA product code for Medical Face Masks, Model Name:MY020003 is FXX.

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医療用フェイスマスク、モデル名：MY020003

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：FXX）

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