FDA 510(k)

InnovaMatrix

K 號：K193552 · 2020-10-21

決定日期2020-10-21

產品代碼KGN

決定相當於

器材摘要

InnovaMatrix 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 2020-10-21 under 510(k) number K193552. The device is classified under product code KGN. FDA Decision: Substantially Equivalent.

常見問題

What is the InnovaMatrix?

InnovaMatrix is a medical device that received FDA 510(k) clearance on 2020-10-21. The listed applicant is Triad Life Sciences, Inc.. The 510(k) number is K193552.

When did InnovaMatrix receive FDA 510(k) clearance?

InnovaMatrix received FDA 510(k) clearance on 2020-10-21, under 510(k) number K193552.

Who is the listed applicant for InnovaMatrix?

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?

The FDA product code for InnovaMatrix 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 K210580InnovaMatrix FS

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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