FDA 510(k)

Remunity 泵用於Remodulin（treprostinil）注射劑

K 號：K202690 · 2020-12-30

決定日期2020-12-30

產品代碼QJY

諮詢委員會醫療設備規範文本翻譯如下： HO 注意：原文中未提供具體的醫療設備規範文本，因此上述翻譯僅為示例。請提供完整的規範文本以便進行準確翻譯。

決定相當於

器材摘要

Remunity Pump for Remodulin (treprostinil) Injection is the device name listed in this FDA 510(k) record. The listed applicant is Deka Research and Development. It received FDA 510(k) clearance on 2020-12-30 under 510(k) number K202690. The device is classified under product code QJY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Remunity Pump for Remodulin (treprostinil) Injection?

Remunity Pump for Remodulin (treprostinil) Injection is a medical device that received FDA 510(k) clearance on 2020-12-30. The listed applicant is Deka Research and Development. The 510(k) number is K202690.

When did Remunity Pump for Remodulin (treprostinil) Injection receive FDA 510(k) clearance?

Remunity Pump for Remodulin (treprostinil) Injection received FDA 510(k) clearance on 2020-12-30, under 510(k) number K202690.

Who is the listed applicant for Remunity Pump for Remodulin (treprostinil) Injection?

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

What is the FDA product code for Remunity Pump for Remodulin (treprostinil) Injection?

The FDA product code for Remunity Pump for Remodulin (treprostinil) Injection is QJY.

其他以 Deka Research and Development 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：QJY）

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。

K243354Remunity 系統Deka Research & Development Corp.K240256Remunity 系統Deka Research and Development K191313Unity 皮下单室輸注系統用於RemodulinDEKA Research & Development

官方來源

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