FDA 510(k)

心輝 Aimigo 配備 12-L 心電圖合成軟體系統

K 號：K250258 · 2025-12-08

決定日期2025-12-08

產品代碼DXH

諮詢委員會履歷

決定相當於

器材摘要

HeartBeam AIMIGo with 12-L ECG Synthesis Software System is the device name listed in this FDA 510(k) record. The listed applicant is Heartbeam, Inc.. It received FDA 510(k) clearance on 2025-12-08 under 510(k) number K250258. The device is classified under product code DXH. It was reviewed by the CV advisory panel. Product code DXH falls under the category of Hematology, which includes devices for blood cell counting, coagulation testing, and hemoglobin analysis. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

常見問題

What is the HeartBeam AIMIGo with 12-L ECG Synthesis Software System?

HeartBeam AIMIGo with 12-L ECG Synthesis Software System is a medical device that received FDA 510(k) clearance on 2025-12-08. The listed applicant is Heartbeam, Inc.. The 510(k) number is K250258.

When did HeartBeam AIMIGo with 12-L ECG Synthesis Software System receive FDA 510(k) clearance?

HeartBeam AIMIGo with 12-L ECG Synthesis Software System received FDA 510(k) clearance on 2025-12-08, under 510(k) number K250258.

Who is the listed applicant for HeartBeam AIMIGo with 12-L ECG Synthesis Software System?

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

What is the FDA product code for HeartBeam AIMIGo with 12-L ECG Synthesis Software System?

The FDA product code for HeartBeam AIMIGo with 12-L ECG Synthesis Software System is DXH. This falls under the Hematology category.

其他以 Heartbeam, Inc. 為申請人之記錄

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相關器械（代碼：DXH）

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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