FDA 510(k)

NG輸送導管

K 號：K230609 · 2023-09-13

決定日期2023-09-13

產品代碼QJP

諮詢委員會履歷

決定相當於

器材摘要

NG Delivery Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Balt USA, LLC. It received FDA 510(k) clearance on 2023-09-13 under 510(k) number K230609. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the NG Delivery Catheter?

NG Delivery Catheter is a medical device that received FDA 510(k) clearance on 2023-09-13. The listed applicant is Balt USA, LLC. The 510(k) number is K230609.

When did NG Delivery Catheter receive FDA 510(k) clearance?

NG Delivery Catheter received FDA 510(k) clearance on 2023-09-13, under 510(k) number K230609.

Who is the listed applicant for NG Delivery Catheter?

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

What is the FDA product code for NG Delivery Catheter?

The FDA product code for NG Delivery Catheter is QJP.

其他以 Balt USA, LLC 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。

K260199SLIM 微导管 K254223下一代 088 管子 K254221Optima 結構系統（OptiOne 結構系統）K252569載體XL輸送導管 K252700Optima 結構系統（Optima 包裝結構系統）K243948Raptor 吸引針管；Balt 吸引管路組

查看所有 19 項裝置 →

相關器械（代碼：QJP）

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。

K260220路92醫療全長046進入系統Route 92 Medical, Inc.K26227770 神經導引針管Piraeus Medical, Inc.K261176Zoom 4S 管針Imperative Care, Inc.K254071p17 XR 微导管Wallaby Medical K260199SLIM 微导管Balt USA, LLC K253901蟻蟻88 接通導管Perfuze, Ltd.

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。