FDA 510(k)

HP PRO 定位設備

K 號：K171734 · 2017-07-25

決定日期2017-07-25

產品代碼IYE

諮詢委員會RA

決定相當於

器材摘要

HP PRO Positioning Device is the device name listed in this FDA 510(k) record. The listed applicant is Orfit Industries NV. It received FDA 510(k) clearance on 2017-07-25 under 510(k) number K171734. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the HP PRO Positioning Device?

HP PRO Positioning Device is a medical device that received FDA 510(k) clearance on 2017-07-25. The listed applicant is Orfit Industries NV. The 510(k) number is K171734.

When did HP PRO Positioning Device receive FDA 510(k) clearance?

HP PRO Positioning Device received FDA 510(k) clearance on 2017-07-25, under 510(k) number K171734.

Who is the listed applicant for HP PRO Positioning Device?

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

What is the FDA product code for HP PRO Positioning Device?

The FDA product code for HP PRO Positioning Device is IYE.

其他以 Orfit Industries NV 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：IYE）

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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