FDA 510(k)

數位ClarusScope系統及數位NeuroPEN系統

K 號：K252790 · 2026-05-26

決定日期2026-05-26

產品代碼HRX

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決定相當於

器材摘要

Digital ClarusScope System and Digital NeuroPEN System is the device name listed in this FDA 510(k) record. The listed applicant is Clarus Medical, LLC. It received FDA 510(k) clearance on 2026-05-26 under 510(k) number K252790. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Digital ClarusScope System and Digital NeuroPEN System?

Digital ClarusScope System and Digital NeuroPEN System is a medical device that received FDA 510(k) clearance on 2026-05-26. The listed applicant is Clarus Medical, LLC. The 510(k) number is K252790.

When did Digital ClarusScope System and Digital NeuroPEN System receive FDA 510(k) clearance?

Digital ClarusScope System and Digital NeuroPEN System received FDA 510(k) clearance on 2026-05-26, under 510(k) number K252790.

Who is the listed applicant for Digital ClarusScope System and Digital NeuroPEN System?

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

What is the FDA product code for Digital ClarusScope System and Digital NeuroPEN System?

The FDA product code for Digital ClarusScope System and Digital NeuroPEN System is HRX.

其他以 Clarus Medical, LLC 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。

K240535Digital ClarusScope 系統；Digital NeuroPEN 系統 K223615數位克拉斯斯科普系統，數位神經筆系統 K200925Clarus 抽離導管套管

相關器械（代碼：HRX）

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。

K260203富麗椎體成形術氣球針管Beijing Fule Science & Technology Development Co., Ltd.K254103霍普金斯內視鏡術望遠鏡Karl Storz SE & CO. KG K253523Freedom DS™ 解壓系統Spinal Simplicity K252546Vantage™ 腰椎减压套件Allevion Medical, LLC K253217MiiS Horus 鼻喉鏡 (EJA 100)；MiiS Horus 結腸鏡顯示系統 - 平板 (EDS 500)；MiiS Horus 結腸鏡顯示系統 - 遙控盒 (EVS 700)Medimaging Integrated Solution, Inc (Miis)K250795PUREVUE™ FMSW.O.M. World of Medicine GmbH

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