FDA 510(k)

Vevazz LED

K 號：K172111 · 2017-11-22

決定日期2017-11-22

產品代碼OLI

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

Vevazz LED is the device name listed in this FDA 510(k) record. The listed applicant is Vevazz, LLC. It received FDA 510(k) clearance on 2017-11-22 under 510(k) number K172111. The device is classified under product code OLI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Vevazz LED?

Vevazz LED is a medical device that received FDA 510(k) clearance on 2017-11-22. The listed applicant is Vevazz, LLC. The 510(k) number is K172111.

When did Vevazz LED receive FDA 510(k) clearance?

Vevazz LED received FDA 510(k) clearance on 2017-11-22, under 510(k) number K172111.

Who is the listed applicant for Vevazz LED?

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

What is the FDA product code for Vevazz LED?

The FDA product code for Vevazz LED is OLI.

其他以 Vevazz, LLC 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。

K162763Vevazz 過濾式LED熱燈

相關器械（代碼：OLI）

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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