FDA 510(k)

Maxxi Rip 感測器

K 號：K171304 · 2019-06-24

決定日期2019-06-24

產品代碼MNR

諮詢委員會AN

決定相當於

器材摘要

Maxxi Rip Sensor is the device name listed in this FDA 510(k) record. The listed applicant is Neurovirtual USA, Inc.. It received FDA 510(k) clearance on 2019-06-24 under 510(k) number K171304. The device is classified under product code MNR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Maxxi Rip Sensor?

Maxxi Rip Sensor is a medical device that received FDA 510(k) clearance on 2019-06-24. The listed applicant is Neurovirtual USA, Inc.. The 510(k) number is K171304.

When did Maxxi Rip Sensor receive FDA 510(k) clearance?

Maxxi Rip Sensor received FDA 510(k) clearance on 2019-06-24, under 510(k) number K171304.

Who is the listed applicant for Maxxi Rip Sensor?

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

What is the FDA product code for Maxxi Rip Sensor?

The FDA product code for Maxxi Rip Sensor is MNR.

其他以 Neurovirtual USA, Inc. 為申請人之記錄

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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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