FDA 510(k)

iCEWav神經監測平台

K 號：K191868 · 2020-03-31

決定日期2020-03-31

產品代碼GWQ

諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

iCEWav Neuromonitoring Platform is the device name listed in this FDA 510(k) record. The listed applicant is Ice Neurosystems, Inc.. It received FDA 510(k) clearance on 2020-03-31 under 510(k) number K191868. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the iCEWav Neuromonitoring Platform?

iCEWav Neuromonitoring Platform is a medical device that received FDA 510(k) clearance on 2020-03-31. The listed applicant is Ice Neurosystems, Inc.. The 510(k) number is K191868.

When did iCEWav Neuromonitoring Platform receive FDA 510(k) clearance?

iCEWav Neuromonitoring Platform received FDA 510(k) clearance on 2020-03-31, under 510(k) number K191868.

Who is the listed applicant for iCEWav Neuromonitoring Platform?

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

What is the FDA product code for iCEWav Neuromonitoring Platform?

The FDA product code for iCEWav Neuromonitoring Platform is GWQ.

其他以 Ice Neurosystems, Inc. 為申請人之記錄

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相關器械（代碼：GWQ）

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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