FDA 510(k)

通氣安瓿瓶轉接器傳遞設備 - 13mm

K 號：K160503 · 2016-05-04

決定日期2016-05-04

產品代碼LHI

諮詢委員會醫療設備規範文本翻譯如下： HO 注意：原文中未提供具體的醫療設備規範文本，因此上述翻譯僅為示例。請提供完整的規範文本以便進行準確翻譯。

決定相當於

器材摘要

Vented Vial Adapter Transfer Device - 13mm is the device name listed in this FDA 510(k) record. The listed applicant is Medimop Medical Projects, Ltd.. It received FDA 510(k) clearance on 2016-05-04 under 510(k) number K160503. The device is classified under product code LHI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Vented Vial Adapter Transfer Device - 13mm?

Vented Vial Adapter Transfer Device - 13mm is a medical device that received FDA 510(k) clearance on 2016-05-04. The listed applicant is Medimop Medical Projects, Ltd.. The 510(k) number is K160503.

When did Vented Vial Adapter Transfer Device - 13mm receive FDA 510(k) clearance?

Vented Vial Adapter Transfer Device - 13mm received FDA 510(k) clearance on 2016-05-04, under 510(k) number K160503.

Who is the listed applicant for Vented Vial Adapter Transfer Device - 13mm?

The FDA 510(k) record lists Medimop Medical Projects, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vented Vial Adapter Transfer Device - 13mm?

The FDA product code for Vented Vial Adapter Transfer Device - 13mm is LHI.

相關器械（代碼：LHI）

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官方來源

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器材摘要

常見問題

相關臨床試驗

相關器械（代碼：LHI）

官方來源