FDA 510(k)

合併通用視覺器（MUV）

K 號：K250301 · 2025-04-14

決定日期2025-04-14

產品代碼LLZ

諮詢委員會RA

決定相當於

器材摘要

Merge Universal Viewer (MUV) is the device name listed in this FDA 510(k) record. The listed applicant is Merge Healthcare Incorporated. It received FDA 510(k) clearance on 2025-04-14 under 510(k) number K250301. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Merge Universal Viewer (MUV)?

Merge Universal Viewer (MUV) is a medical device that received FDA 510(k) clearance on 2025-04-14. The listed applicant is Merge Healthcare Incorporated. The 510(k) number is K250301.

When did Merge Universal Viewer (MUV) receive FDA 510(k) clearance?

Merge Universal Viewer (MUV) received FDA 510(k) clearance on 2025-04-14, under 510(k) number K250301.

Who is the listed applicant for Merge Universal Viewer (MUV)?

The FDA 510(k) record lists Merge Healthcare Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Merge Universal Viewer (MUV)?

The FDA product code for Merge Universal Viewer (MUV) is LLZ.

其他以 Merge Healthcare Incorporated 為申請人之記錄

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K233326合併Hemo，型號RCSV2 K203104IBM iConnect Access K192455合併PACS K192276合併心臟設備醫療設備規範文本合併心臟設備 FDA（美國食品藥品管理局） 510(k)（美國食品藥品管理局的510(k)認證程序） PMA（美國食品藥品管理局的上市前批准） NCT（臨床試驗登錄號） PMID（PubMed標識符）識別碼網址政策：醫療規範-v1 K182290IBM iConnect Access K173475合併PACS

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相關器械（代碼：LLZ）

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。

K261874Syneris PACS v.1.0.1.0Syneris K262442HipStudio分析Replasia BV K261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

官方來源

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