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FDA 510(k)

Vas-Q-Clip

K 號:K151943 · 2016-03-25

決定日期2016-03-25
產品代碼FZP
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

Vas-Q-Clip is the device name listed in this FDA 510(k) record. The listed applicant is Nanova Biomaterials, Inc.. It received FDA 510(k) clearance on 2016-03-25 under 510(k) number K151943. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Vas-Q-Clip?

Vas-Q-Clip is a medical device that received FDA 510(k) clearance on 2016-03-25. The listed applicant is Nanova Biomaterials, Inc.. The 510(k) number is K151943.

When did Vas-Q-Clip receive FDA 510(k) clearance?

Vas-Q-Clip received FDA 510(k) clearance on 2016-03-25, under 510(k) number K151943.

Who is the listed applicant for Vas-Q-Clip?

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

What is the FDA product code for Vas-Q-Clip?

The FDA product code for Vas-Q-Clip is FZP.

其他以 Nanova Biomaterials, Inc. 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。

相關器械(代碼:FZP)

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。

官方來源

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