FDA 510(k)

Altaviz Needle Kit II

K 號：K231261 · 2023-07-27

決定日期2023-07-27

產品代碼FMI

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

Altaviz Needle Kit II is the device name listed in this FDA 510(k) record. The listed applicant is Altaviz, LLC. It received FDA 510(k) clearance on 2023-07-27 under 510(k) number K231261. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Altaviz Needle Kit II?

Altaviz Needle Kit II is a medical device that received FDA 510(k) clearance on 2023-07-27. The listed applicant is Altaviz, LLC. The 510(k) number is K231261.

When did Altaviz Needle Kit II receive FDA 510(k) clearance?

Altaviz Needle Kit II received FDA 510(k) clearance on 2023-07-27, under 510(k) number K231261.

Who is the listed applicant for Altaviz Needle Kit II?

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

What is the FDA product code for Altaviz Needle Kit II?

The FDA product code for Altaviz Needle Kit II is FMI.

其他以 Altaviz, LLC 為申請人之記錄

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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相關器械（代碼：FMI）

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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