FDA 510(k)

藍星及藍星Rx

K 號：K230813 · 2023-07-28

決定日期2023-07-28

產品代碼NDC

諮詢委員會AN

決定相當於

器材摘要

BlueStar and BlueStar Rx is the device name listed in this FDA 510(k) record. The listed applicant is Welldoc, Inc.. It received FDA 510(k) clearance on 2023-07-28 under 510(k) number K230813. The device is classified under product code NDC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the BlueStar and BlueStar Rx?

BlueStar and BlueStar Rx is a medical device that received FDA 510(k) clearance on 2023-07-28. The listed applicant is Welldoc, Inc.. The 510(k) number is K230813.

When did BlueStar and BlueStar Rx receive FDA 510(k) clearance?

BlueStar and BlueStar Rx received FDA 510(k) clearance on 2023-07-28, under 510(k) number K230813.

Who is the listed applicant for BlueStar and BlueStar Rx?

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

What is the FDA product code for BlueStar and BlueStar Rx?

The FDA product code for BlueStar and BlueStar Rx is NDC.

其他以 Welldoc, 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。

K222888藍星CGM胰島素劑量計算器 K203434藍星藥妝 K193654藍星藥妝 K190013WellDoc 藍星 K162532WellDoc 藍星，WellDoc 藍星藥妝 K162225WellDoc 藍星（WellDoc 糖尿病管理系統及糖尿病管理-Rx 系統）

查看所有 7 項裝置 →

相關器械（代碼：NDC）

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。

K254102GlucommanderGlytec, LLC K260910EndoTool IV雲端 1.0Glooko, Inc.K253512迷你美迪 Go AppMedtronic Minimed K253281上醫材Updoc, Inc.K252104T1D1Comerge AG K241088EndoTool IV (3.1)Monarch Medical Technologies

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。