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FDA 510(k)

VitalSigns 1-Lead Holter (VSH101)

K 號:K243003 · 2025-06-17

決定日期2025-06-17
產品代碼DXH
諮詢委員會履歷
決定相當於

器材摘要

VitalSigns 1-Lead Holter (VSH101) is the device name listed in this FDA 510(k) record. The listed applicant is VitalSigns Technology Co., Ltd.. It received FDA 510(k) clearance on 2025-06-17 under 510(k) number K243003. 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 VitalSigns 1-Lead Holter (VSH101)?

VitalSigns 1-Lead Holter (VSH101) is a medical device that received FDA 510(k) clearance on 2025-06-17. The listed applicant is VitalSigns Technology Co., Ltd.. The 510(k) number is K243003.

When did VitalSigns 1-Lead Holter (VSH101) receive FDA 510(k) clearance?

VitalSigns 1-Lead Holter (VSH101) received FDA 510(k) clearance on 2025-06-17, under 510(k) number K243003.

Who is the listed applicant for VitalSigns 1-Lead Holter (VSH101)?

The FDA 510(k) record lists VitalSigns Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VitalSigns 1-Lead Holter (VSH101)?

The FDA product code for VitalSigns 1-Lead Holter (VSH101) is DXH. This falls under the Hematology category.

相關臨床試驗

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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。

官方來源

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