FDA 510(k)

PM2+系統及SmartPICC針筒

K 號：K243484 · 2025-05-29

決定日期2025-05-29

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 and SmartPICC Stylet 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 2025-05-29 under 510(k) number K243484. 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 and SmartPICC Stylet?

PM2+ System and SmartPICC Stylet is a medical device that received FDA 510(k) clearance on 2025-05-29. The listed applicant is Piccolo Medical, Inc.. The 510(k) number is K243484.

When did PM2+ System and SmartPICC Stylet receive FDA 510(k) clearance?

PM2+ System and SmartPICC Stylet received FDA 510(k) clearance on 2025-05-29, under 510(k) number K243484.

Who is the listed applicant for PM2+ System and SmartPICC Stylet?

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 and SmartPICC Stylet?

The FDA product code for PM2+ System and SmartPICC Stylet 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。

K252792PM2™ 系統搭配 ECGuide™ 接頭 K240486PM2系統及EC導引連接器 K200037皮科醫療智慧PICC系統

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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