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FDA 510(k)

All-in-One Health Monitor, PC-303

K 號:K170047 · 2017-09-09

決定日期2017-09-09
產品代碼MWI
諮詢委員會履歷
決定相當於

器材摘要

All-in-One Health Monitor, PC-303 is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Creative Industry Co., Ltd.. It received FDA 510(k) clearance on 2017-09-09 under 510(k) number K170047. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the All-in-One Health Monitor, PC-303?

All-in-One Health Monitor, PC-303 is a medical device that received FDA 510(k) clearance on 2017-09-09. The listed applicant is Shenzhen Creative Industry Co., Ltd.. The 510(k) number is K170047.

When did All-in-One Health Monitor, PC-303 receive FDA 510(k) clearance?

All-in-One Health Monitor, PC-303 received FDA 510(k) clearance on 2017-09-09, under 510(k) number K170047.

Who is the listed applicant for All-in-One Health Monitor, PC-303?

The FDA 510(k) record lists Shenzhen Creative Industry Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for All-in-One Health Monitor, PC-303?

The FDA product code for All-in-One Health Monitor, PC-303 is MWI.

相關臨床試驗

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其他以 Shenzhen Creative Industry Co., Ltd. 為申請人之記錄

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相關器械(代碼:MWI)

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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