FDA 510(k)

Eusol-C

K 號：K162013 · 2016-09-15

決定日期2016-09-15

產品代碼LYX

決定相當於

器材摘要

Eusol-C is the device name listed in this FDA 510(k) record. The listed applicant is Al.Chi.Mi.A. S.R.L. It received FDA 510(k) clearance on 2016-09-15 under 510(k) number K162013. The device is classified under product code LYX. FDA Decision: Substantially Equivalent.

常見問題

What is the Eusol-C?

Eusol-C is a medical device that received FDA 510(k) clearance on 2016-09-15. The listed applicant is Al.Chi.Mi.A. S.R.L. The 510(k) number is K162013.

When did Eusol-C receive FDA 510(k) clearance?

Eusol-C received FDA 510(k) clearance on 2016-09-15, under 510(k) number K162013.

Who is the listed applicant for Eusol-C?

The FDA 510(k) record lists Al.Chi.Mi.A. S.R.L as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Eusol-C?

The FDA product code for Eusol-C is LYX.

其他以 Al.Chi.Mi.A. S.R.L 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。

K251320XTRA4

相關器械（代碼：LYX）

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。

K251320XTRA4Al.Chi.Mi.A. S.R.L K221759科尼索爾Aurolab K211786獨立角膜觀察室（IVC-21）Bausch + Lomb, Incorporated

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。