FDA 510(k)

LIVIA

K 號：K183110 · 2020-05-04

決定日期2020-05-04

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

LIVIA is the device name listed in this FDA 510(k) record. The listed applicant is Lifecare , Ltd.. It received FDA 510(k) clearance on 2020-05-04 under 510(k) number K183110. 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 LIVIA?

LIVIA is a medical device that received FDA 510(k) clearance on 2020-05-04. The listed applicant is Lifecare , Ltd.. The 510(k) number is K183110.

When did LIVIA receive FDA 510(k) clearance?

LIVIA received FDA 510(k) clearance on 2020-05-04, under 510(k) number K183110.

Who is the listed applicant for LIVIA?

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

What is the FDA product code for LIVIA?

The FDA product code for LIVIA is NUH.

其他以 Lifecare , Ltd. 為申請人之記錄

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K163153麗薇雅

相關器械（代碼：NUH）

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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