FDA 510(k)

LVivo 無縫

K 號：K243331 · 2025-03-06

決定日期2025-03-06

產品代碼QIH

諮詢委員會RA

決定相當於

器材摘要

LVivo Seamless is the device name listed in this FDA 510(k) record. The listed applicant is Dia Imaging Analysis, Ltd.. It received FDA 510(k) clearance on 2025-03-06 under 510(k) number K243331. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the LVivo Seamless?

LVivo Seamless is a medical device that received FDA 510(k) clearance on 2025-03-06. The listed applicant is Dia Imaging Analysis, Ltd.. The 510(k) number is K243331.

When did LVivo Seamless receive FDA 510(k) clearance?

LVivo Seamless received FDA 510(k) clearance on 2025-03-06, under 510(k) number K243331.

Who is the listed applicant for LVivo Seamless?

The FDA 510(k) record lists Dia Imaging Analysis, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LVivo Seamless?

The FDA product code for LVivo Seamless is QIH.

其他以 Dia Imaging Analysis, Ltd. 為申請人之記錄

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相關器械（代碼：QIH）

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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