FDA 510(k)

Sample Preservative Fluid

K番号: K222771 · 2024-06-26

決定日2024-06-26

製品コードQBD

諮問委員会以下は、提供された医療機器規制テキストの日本語訳です。 --- MI --- URLや識別子などは原文のままです。

決定Substantially Equivalent

医療機器の概要

Sample Preservative Fluid is the device name listed in this FDA 510(k) record. The listed applicant is Hangzhou Bioer Technology Co., Ltd.. It received FDA 510(k) clearance on 2024-06-26 under 510(k) number K222771. The device is classified under product code QBD. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Sample Preservative Fluid?

Sample Preservative Fluid is a medical device that received FDA 510(k) clearance on 2024-06-26. The listed applicant is Hangzhou Bioer Technology Co., Ltd.. The 510(k) number is K222771.

When did Sample Preservative Fluid receive FDA 510(k) clearance?

Sample Preservative Fluid received FDA 510(k) clearance on 2024-06-26, under 510(k) number K222771.

Who is the listed applicant for Sample Preservative Fluid?

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

What is the FDA product code for Sample Preservative Fluid?

The FDA product code for Sample Preservative Fluid is QBD.

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Sample Preservative Fluid

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：QBD）

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