FDA 510(k)

CS 9600

K 號：K200183 · 2020-03-13

申請人Trophy

決定日期2020-03-13

產品代碼OAS

諮詢委員會RA

決定相當於

器材摘要

CS 9600 is the device name listed in this FDA 510(k) record. The listed applicant is Trophy. It received FDA 510(k) clearance on 2020-03-13 under 510(k) number K200183. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the CS 9600?

CS 9600 is a medical device that received FDA 510(k) clearance on 2020-03-13. The listed applicant is Trophy. The 510(k) number is K200183.

When did CS 9600 receive FDA 510(k) clearance?

CS 9600 received FDA 510(k) clearance on 2020-03-13, under 510(k) number K200183.

Who is the listed applicant for CS 9600?

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

What is the FDA product code for CS 9600?

The FDA product code for CS 9600 is OAS.

其他以 Trophy 為申請人之記錄

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相關器械（代碼：OAS）

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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