FDA 510(k)

Hybrid3D

K 號：K163394 · 2017-05-22

決定日期2017-05-22

產品代碼KPS

諮詢委員會RA

決定相當於

器材摘要

Hybrid3D is the device name listed in this FDA 510(k) record. The listed applicant is Hermes Medical Solutions AB. It received FDA 510(k) clearance on 2017-05-22 under 510(k) number K163394. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Hybrid3D?

Hybrid3D is a medical device that received FDA 510(k) clearance on 2017-05-22. The listed applicant is Hermes Medical Solutions AB. The 510(k) number is K163394.

When did Hybrid3D receive FDA 510(k) clearance?

Hybrid3D received FDA 510(k) clearance on 2017-05-22, under 510(k) number K163394.

Who is the listed applicant for Hybrid3D?

FDA 510(k) 記錄將 Hermes Medical Solutions AB 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Hybrid3D?

The FDA product code for Hybrid3D is KPS.

其他以 Hermes Medical Solutions AB 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：KPS）

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。

官方來源

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