FDA 510(k)

無線電纜

K 號：K152826 · 2016-05-27

決定日期2016-05-27

產品代碼ELW

諮詢委員會DE

決定相當於

器材摘要

NoCord is the device name listed in this FDA 510(k) record. The listed applicant is Centrix, Inc.. It received FDA 510(k) clearance on 2016-05-27 under 510(k) number K152826. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the NoCord?

NoCord is a medical device that received FDA 510(k) clearance on 2016-05-27. The listed applicant is Centrix, Inc.. The 510(k) number is K152826.

When did NoCord receive FDA 510(k) clearance?

NoCord received FDA 510(k) clearance on 2016-05-27, under 510(k) number K152826.

Who is the listed applicant for NoCord?

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

What is the FDA product code for NoCord?

The FDA product code for NoCord is ELW.

其他以 Centrix, Inc. 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。

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相關器械（代碼：ELW）

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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