FDA 510(k)

科結微

K 號：K202551 · 2021-06-24

決定日期2021-06-24

產品代碼GCJ

諮詢委員會GU

決定相當於

器材摘要

Cor-Knot Micro is the device name listed in this FDA 510(k) record. The listed applicant is Lsi Solutions, Inc.. It received FDA 510(k) clearance on 2021-06-24 under 510(k) number K202551. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Cor-Knot Micro?

Cor-Knot Micro is a medical device that received FDA 510(k) clearance on 2021-06-24. The listed applicant is Lsi Solutions, Inc.. The 510(k) number is K202551.

When did Cor-Knot Micro receive FDA 510(k) clearance?

Cor-Knot Micro received FDA 510(k) clearance on 2021-06-24, under 510(k) number K202551.

Who is the listed applicant for Cor-Knot Micro?

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

What is the FDA product code for Cor-Knot Micro?

The FDA product code for Cor-Knot Micro is GCJ.

其他以 Lsi Solutions, 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：GCJ）

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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