FDA 510(k)

Correx軟體

K 號：K212552 · 2021-10-12

決定日期2021-10-12

產品代碼KTT

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決定相當於

器材摘要

Correx Software is the device name listed in this FDA 510(k) record. The listed applicant is Vilex, LLC. It received FDA 510(k) clearance on 2021-10-12 under 510(k) number K212552. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Correx Software?

Correx Software is a medical device that received FDA 510(k) clearance on 2021-10-12. The listed applicant is Vilex, LLC. The 510(k) number is K212552.

When did Correx Software receive FDA 510(k) clearance?

Correx Software received FDA 510(k) clearance on 2021-10-12, under 510(k) number K212552.

Who is the listed applicant for Correx Software?

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

What is the FDA product code for Correx Software?

The FDA product code for Correx Software is KTT.

其他以 Vilex, 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。

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相關器械（代碼：KTT）

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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