FDA 510(k)

再處理式電剃刀/磨頭

K 號：K172092 · 2017-10-04

決定日期2017-10-04

產品代碼HRX

諮詢委員會或

決定相當於

器材摘要

Reprocessed Shavers/Burs is the device name listed in this FDA 510(k) record. The listed applicant is Renovo, Inc.. It received FDA 510(k) clearance on 2017-10-04 under 510(k) number K172092. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Reprocessed Shavers/Burs?

Reprocessed Shavers/Burs is a medical device that received FDA 510(k) clearance on 2017-10-04. The listed applicant is Renovo, Inc.. The 510(k) number is K172092.

When did Reprocessed Shavers/Burs receive FDA 510(k) clearance?

Reprocessed Shavers/Burs received FDA 510(k) clearance on 2017-10-04, under 510(k) number K172092.

Who is the listed applicant for Reprocessed Shavers/Burs?

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

What is the FDA product code for Reprocessed Shavers/Burs?

The FDA product code for Reprocessed Shavers/Burs is HRX.

其他以 Renovo, 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：HRX）

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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