FDA 510(k)

Sunmas TENS & PMS（型號 SM9187、SM9180L、SM9180S）

K 號：K190009 · 2019-12-02

申請人Hong Qiangxing (Shenzhen) Electronics Limited

決定日期2019-12-02

產品代碼NUH

諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

Sunmas TENS & PMS (Model SM9187, SM9180L, SM9180S) is the device name listed in this FDA 510(k) record. The listed applicant is Hong Qiangxing (Shenzhen) Electronics Limited. It received FDA 510(k) clearance on 2019-12-02 under 510(k) number K190009. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Sunmas TENS & PMS (Model SM9187, SM9180L, SM9180S)?

Sunmas TENS & PMS (Model SM9187, SM9180L, SM9180S) is a medical device that received FDA 510(k) clearance on 2019-12-02. The listed applicant is Hong Qiangxing (Shenzhen) Electronics Limited. The 510(k) number is K190009.

When did Sunmas TENS & PMS (Model SM9187, SM9180L, SM9180S) receive FDA 510(k) clearance?

Sunmas TENS & PMS (Model SM9187, SM9180L, SM9180S) received FDA 510(k) clearance on 2019-12-02, under 510(k) number K190009.

Who is the listed applicant for Sunmas TENS & PMS (Model SM9187, SM9180L, SM9180S)?

The FDA 510(k) record lists Hong Qiangxing (Shenzhen) Electronics Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sunmas TENS & PMS (Model SM9187, SM9180L, SM9180S)?

The FDA product code for Sunmas TENS & PMS (Model SM9187, SM9180L, SM9180S) is NUH.

其他以 Hong Qiangxing (Shenzhen) Electronics Limited 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：NUH）

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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