FDA 510(k)

WiTouch Pro、WiTouch、Neubac

K 號：K171599 · 2017-09-22

決定日期2017-09-22

產品代碼NUH

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

WiTouch Pro, WiTouch, Neubac is the device name listed in this FDA 510(k) record. The listed applicant is Hollywog, LLC. It received FDA 510(k) clearance on 2017-09-22 under 510(k) number K171599. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the WiTouch Pro, WiTouch, Neubac?

WiTouch Pro, WiTouch, Neubac is a medical device that received FDA 510(k) clearance on 2017-09-22. The listed applicant is Hollywog, LLC. The 510(k) number is K171599.

When did WiTouch Pro, WiTouch, Neubac receive FDA 510(k) clearance?

WiTouch Pro, WiTouch, Neubac received FDA 510(k) clearance on 2017-09-22, under 510(k) number K171599.

Who is the listed applicant for WiTouch Pro, WiTouch, Neubac?

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

What is the FDA product code for WiTouch Pro, WiTouch, Neubac?

The FDA product code for WiTouch Pro, WiTouch, Neubac is NUH.

相關器械（代碼：NUH）

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器材摘要

常見問題

相關臨床試驗

相關器械（代碼：NUH）

官方來源