FDA 510(k)

VSP系統

K 號：K192192 · 2020-02-26

決定日期2020-02-26

產品代碼DZJ

諮詢委員會DE

決定相當於

器材摘要

VSP System is the device name listed in this FDA 510(k) record. The listed applicant is 3D Systems. It received FDA 510(k) clearance on 2020-02-26 under 510(k) number K192192. The device is classified under product code DZJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the VSP System?

VSP System is a medical device that received FDA 510(k) clearance on 2020-02-26. The listed applicant is 3D Systems. The 510(k) number is K192192.

When did VSP System receive FDA 510(k) clearance?

VSP System received FDA 510(k) clearance on 2020-02-26, under 510(k) number K192192.

Who is the listed applicant for VSP System?

The FDA 510(k) record lists 3D Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VSP System?

The FDA product code for VSP System is DZJ.

其他以 3D Systems 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：DZJ）

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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