免責聲明: 本站彙整 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公開資料,僅供一般參考,不構成醫療建議、診斷、治療建議或投資建議。

FDA 510(k)

TENS & PMS(型號:SM9089、SM9587、SM9592、SM9555)

K 號:K220152 · 2022-04-19

決定日期2022-04-19
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

TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555) 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 2022-04-19 under 510(k) number K220152. 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 TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555)?

TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555) is a medical device that received FDA 510(k) clearance on 2022-04-19. The listed applicant is Hong Qiangxing (Shenzhen) Electronics Limited. The 510(k) number is K220152.

When did TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555) receive FDA 510(k) clearance?

TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555) received FDA 510(k) clearance on 2022-04-19, under 510(k) number K220152.

Who is the listed applicant for TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555)?

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 TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555)?

The FDA product code for TENS & PMS (Model:SM9089, SM9587, SM9592, SM9555) is NUH.

相關臨床試驗

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。

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。

查看所有 7 項裝置 →

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。

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊,請始終參閱官方記錄。

↑