FDA 510(k)

圖博特儀器模組

K 號：K200240 · 2020-04-30

決定日期2020-04-30

產品代碼FRG

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

Turbett Instrument Pod is the device name listed in this FDA 510(k) record. The listed applicant is Turbett Surgical, Inc.. It received FDA 510(k) clearance on 2020-04-30 under 510(k) number K200240. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Turbett Instrument Pod?

Turbett Instrument Pod is a medical device that received FDA 510(k) clearance on 2020-04-30. The listed applicant is Turbett Surgical, Inc.. The 510(k) number is K200240.

When did Turbett Instrument Pod receive FDA 510(k) clearance?

Turbett Instrument Pod received FDA 510(k) clearance on 2020-04-30, under 510(k) number K200240.

Who is the listed applicant for Turbett Instrument Pod?

The FDA 510(k) record lists Turbett Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Turbett Instrument Pod?

The FDA product code for Turbett Instrument Pod is FRG.

其他以 Turbett Surgical, Inc. 為申請人之記錄

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K202593圖博特儀器模組

相關器械（代碼：FRG）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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