FDA 510(k)

Accuro XV

K 號：K254021 · 2026-04-09

決定日期2026-04-09

產品代碼IYO

諮詢委員會RA

決定相當於

器材摘要

Accuro XV is the device name listed in this FDA 510(k) record. The listed applicant is Rivanna Medical, Inc.. It received FDA 510(k) clearance on 2026-04-09 under 510(k) number K254021. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Accuro XV?

Accuro XV is a medical device that received FDA 510(k) clearance on 2026-04-09. The listed applicant is Rivanna Medical, Inc.. The 510(k) number is K254021.

When did Accuro XV receive FDA 510(k) clearance?

Accuro XV received FDA 510(k) clearance on 2026-04-09, under 510(k) number K254021.

Who is the listed applicant for Accuro XV?

FDA 510(k) 記錄將 Rivanna Medical, Inc. 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Accuro XV?

The FDA product code for Accuro XV is IYO.

其他以 Rivanna 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。

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相關器械（代碼：IYO）

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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