FDA 510(k)

Definium Pace Select

K 號：K231892 · 2023-09-12

決定日期2023-09-12

產品代碼KPR

諮詢委員會RA

決定相當於

器材摘要

Definium Pace Select is the device name listed in this FDA 510(k) record. The listed applicant is Ge Hualun Medical Systems Co. , Ltd.. It received FDA 510(k) clearance on 2023-09-12 under 510(k) number K231892. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Definium Pace Select?

Definium Pace Select is a medical device that received FDA 510(k) clearance on 2023-09-12. The listed applicant is Ge Hualun Medical Systems Co. , Ltd.. The 510(k) number is K231892.

When did Definium Pace Select receive FDA 510(k) clearance?

Definium Pace Select received FDA 510(k) clearance on 2023-09-12, under 510(k) number K231892.

Who is the listed applicant for Definium Pace Select?

The FDA 510(k) record lists Ge Hualun Medical Systems Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Definium Pace Select?

The FDA product code for Definium Pace Select is KPR.

其他以 Ge Hualun Medical Systems Co. , Ltd. 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：KPR）

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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官方來源

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