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FDA 510(k)

喉鏡節段性動脈限制夾 (L-ARC)；動脈限制夾 (ARC)

K 號：K243627 · 2025-12-31

申請人Arc Trauma, LLC
決定日期2025-12-31
產品代碼DXC
諮詢委員會履歷
決定相當於

器材摘要

Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC) is the device name listed in this FDA 510(k) record. The listed applicant is Arc Trauma, LLC. It received FDA 510(k) clearance on 2025-12-31 under 510(k) number K243627. The device is classified under product code DXC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC)?

Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC) is a medical device that received FDA 510(k) clearance on 2025-12-31. The listed applicant is Arc Trauma, LLC. The 510(k) number is K243627.

When did Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC) receive FDA 510(k) clearance?

Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC) received FDA 510(k) clearance on 2025-12-31, under 510(k) number K243627.

Who is the listed applicant for Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC)?

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

What is the FDA product code for Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC)?

The FDA product code for Laryngoscope Junctional-Arterial Restriction Clamp (L-ARC); Arterial Restriction Clamp (ARC) is DXC.

相關臨床試驗

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：DXC）

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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