FDA 510(k)

PM2™ 系統搭配 ECGuide™ 接頭

K 號：K252792 · 2025-11-17

決定日期2025-11-17

產品代碼LJS

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

PM2™ System with ECGuide™ Connector is the device name listed in this FDA 510(k) record. The listed applicant is Piccolo Medical, Inc.. It received FDA 510(k) clearance on 2025-11-17 under 510(k) number K252792. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the PM2™ System with ECGuide™ Connector?

PM2™ System with ECGuide™ Connector is a medical device that received FDA 510(k) clearance on 2025-11-17. The listed applicant is Piccolo Medical, Inc.. The 510(k) number is K252792.

When did PM2™ System with ECGuide™ Connector receive FDA 510(k) clearance?

PM2™ System with ECGuide™ Connector received FDA 510(k) clearance on 2025-11-17, under 510(k) number K252792.

Who is the listed applicant for PM2™ System with ECGuide™ Connector?

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

What is the FDA product code for PM2™ System with ECGuide™ Connector?

The FDA product code for PM2™ System with ECGuide™ Connector is LJS.

其他以 Piccolo Medical, Inc. 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：LJS）

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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