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)

一次性接地垫

K 號:K231985 · 2024-02-16

決定日期2024-02-16
產品代碼GEI
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

Disposable Grounding Pad is the device name listed in this FDA 510(k) record. The listed applicant is Shenzhen Mecun Medical Supply Co., Ltd.. It received FDA 510(k) clearance on 2024-02-16 under 510(k) number K231985. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Disposable Grounding Pad?

Disposable Grounding Pad is a medical device that received FDA 510(k) clearance on 2024-02-16. The listed applicant is Shenzhen Mecun Medical Supply Co., Ltd.. The 510(k) number is K231985.

When did Disposable Grounding Pad receive FDA 510(k) clearance?

Disposable Grounding Pad received FDA 510(k) clearance on 2024-02-16, under 510(k) number K231985.

Who is the listed applicant for Disposable Grounding Pad?

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

What is the FDA product code for Disposable Grounding Pad?

The FDA product code for Disposable Grounding Pad is GEI.

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 Shenzhen Mecun Medical Supply 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。

相關器械(代碼:GEI)

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。

↑