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FDA 510(k)

ProVee影片處理單元(PV-003)

K 號:K251734 · 2025-09-24

決定日期2025-09-24
產品代碼FET
諮詢委員會GU
決定相當於

器材摘要

ProVee Video Processing Unit (PV-003) is the device name listed in this FDA 510(k) record. The listed applicant is Proverum Limited. It received FDA 510(k) clearance on 2025-09-24 under 510(k) number K251734. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ProVee Video Processing Unit (PV-003)?

ProVee Video Processing Unit (PV-003) is a medical device that received FDA 510(k) clearance on 2025-09-24. The listed applicant is Proverum Limited. The 510(k) number is K251734.

When did ProVee Video Processing Unit (PV-003) receive FDA 510(k) clearance?

ProVee Video Processing Unit (PV-003) received FDA 510(k) clearance on 2025-09-24, under 510(k) number K251734.

Who is the listed applicant for ProVee Video Processing Unit (PV-003)?

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

What is the FDA product code for ProVee Video Processing Unit (PV-003)?

The FDA product code for ProVee Video Processing Unit (PV-003) is FET.

相關臨床試驗

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相關器械(代碼:FET)

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。

官方來源

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