FDA 510(k)

MDx-Chex 靈敏測試用於乳癌早期診斷

K 號：K231221 · 2023-07-27

申請人Streck

決定日期2023-07-27

產品代碼PMN

諮詢委員會MI (請提供完整的描述文本，以便進行翻譯。)

決定相當於

器材摘要

MDx-Chex for BC-GP is the device name listed in this FDA 510(k) record. The listed applicant is Streck. It received FDA 510(k) clearance on 2023-07-27 under 510(k) number K231221. The device is classified under product code PMN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MDx-Chex for BC-GP?

MDx-Chex for BC-GP is a medical device that received FDA 510(k) clearance on 2023-07-27. The listed applicant is Streck. The 510(k) number is K231221.

When did MDx-Chex for BC-GP receive FDA 510(k) clearance?

MDx-Chex for BC-GP received FDA 510(k) clearance on 2023-07-27, under 510(k) number K231221.

Who is the listed applicant for MDx-Chex for BC-GP?

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

What is the FDA product code for MDx-Chex for BC-GP?

The FDA product code for MDx-Chex for BC-GP is PMN.

其他以 Streck 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。

K254166MDx-Chex 適用於BCN K231223MDx-Chex 適用於 BC-GN 医療設備規範文本 K170091UA-細胞完整版 K160585XN 藥品設備規範文本 K160590XN檢查 K160588XN檢查BF

查看所有 8 項裝置 →

相關器械（代碼：PMN）

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。

K261475BIOFIRE® FILMARRAY® 熱帶熱症面板控制組Biofire Defense, LLC K260577FilmArray TF 控制面板 M527Maine Molecular Quality Controls, Inc.K260041MDx-Chex 適用於BCPStreck, LLC K254166MDx-Chex 適用於BCNStreck K254167MDx-Chex用於BCY的醫療設備規範文本Streck, LLC K251526FilmArray GI Control Panel M238Maine Molecular Quality Controls, Inc.

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。