FDA 510(k)

無線探頭型超音波掃描儀（型號：UProbe-C；UProbe-L；BProbe）

K 號：K172750 · 2018-02-28

申請人Guangzhou Sonostar Technologies Co., Ltd.

決定日期2018-02-28

產品代碼IYO

諮詢委員會RA

決定相當於

器材摘要

Wireless Probe Type Ultrasound Scanner (Model:UProbe-C; UProbe-L; BProbe) is the device name listed in this FDA 510(k) record. The listed applicant is Guangzhou Sonostar Technologies Co., Ltd.. It received FDA 510(k) clearance on 2018-02-28 under 510(k) number K172750. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Wireless Probe Type Ultrasound Scanner (Model:UProbe-C; UProbe-L; BProbe)?

Wireless Probe Type Ultrasound Scanner (Model:UProbe-C; UProbe-L; BProbe) is a medical device that received FDA 510(k) clearance on 2018-02-28. The listed applicant is Guangzhou Sonostar Technologies Co., Ltd.. The 510(k) number is K172750.

When did Wireless Probe Type Ultrasound Scanner (Model:UProbe-C; UProbe-L; BProbe) receive FDA 510(k) clearance?

Wireless Probe Type Ultrasound Scanner (Model:UProbe-C; UProbe-L; BProbe) received FDA 510(k) clearance on 2018-02-28, under 510(k) number K172750.

Who is the listed applicant for Wireless Probe Type Ultrasound Scanner (Model:UProbe-C; UProbe-L; BProbe)?

The FDA 510(k) record lists Guangzhou Sonostar Technologies Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Wireless Probe Type Ultrasound Scanner (Model:UProbe-C; UProbe-L; BProbe)?

The FDA product code for Wireless Probe Type Ultrasound Scanner (Model:UProbe-C; UProbe-L; BProbe) is IYO.

其他以 Guangzhou Sonostar Technologies Co., Ltd. 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：IYO）

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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