FDA 510(k)

InnovaMatrix FS

K 號：K210580 · 2021-04-21

決定日期2021-04-21

產品代碼KGN

決定相當於

器材摘要

InnovaMatrix FS is the device name listed in this FDA 510(k) record. The listed applicant is Triad Life Sciences, Inc.. It received FDA 510(k) clearance on 2021-04-21 under 510(k) number K210580. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

常見問題

What is the InnovaMatrix FS?

InnovaMatrix FS is a medical device that received FDA 510(k) clearance on 2021-04-21. The listed applicant is Triad Life Sciences, Inc.. The 510(k) number is K210580.

When did InnovaMatrix FS receive FDA 510(k) clearance?

InnovaMatrix FS received FDA 510(k) clearance on 2021-04-21, under 510(k) number K210580.

Who is the listed applicant for InnovaMatrix FS?

The FDA 510(k) record lists Triad Life Sciences, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for InnovaMatrix FS?

The FDA product code for InnovaMatrix FS is KGN.

其他以 Triad Life Sciences, 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。

K213716InnovaBurn K211902InnovaMatrix PD K193552InnovaMatrix

相關器械（代碼：KGN）

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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