FDA 510(k)

Natus 魔法探險者

K 號：K172743 · 2017-12-19

決定日期2017-12-19

產品代碼IKN

諮詢委員會PM

決定相當於

器材摘要

Natus VikingQuest is the device name listed in this FDA 510(k) record. The listed applicant is Natus Neurology Incorporated. It received FDA 510(k) clearance on 2017-12-19 under 510(k) number K172743. The device is classified under product code IKN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Natus VikingQuest?

Natus VikingQuest is a medical device that received FDA 510(k) clearance on 2017-12-19. The listed applicant is Natus Neurology Incorporated. The 510(k) number is K172743.

When did Natus VikingQuest receive FDA 510(k) clearance?

Natus VikingQuest received FDA 510(k) clearance on 2017-12-19, under 510(k) number K172743.

Who is the listed applicant for Natus VikingQuest?

The FDA 510(k) record lists Natus Neurology Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Natus VikingQuest?

The FDA product code for Natus VikingQuest is IKN.

其他以 Natus Neurology Incorporated 為申請人之記錄

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K243982尼可萊特EDX K243495Natus Ultrapro S100 (982A0594)K173366NicoletOne

相關器械（代碼：IKN）

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。

K163150ViMove2Dorsavi, Ltd.K162383Cadwell Sierra Summit, Cadwell Sierra AscentCadwell Industries, Inc.

官方來源

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