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)

神經貼膏

K 號:K210665 · 2022-07-15

決定日期2022-07-15
產品代碼JXI
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

Nerve Tape is the device name listed in this FDA 510(k) record. The listed applicant is Biocircuit Technologies, Incorporated. It received FDA 510(k) clearance on 2022-07-15 under 510(k) number K210665. The device is classified under product code JXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Nerve Tape?

Nerve Tape is a medical device that received FDA 510(k) clearance on 2022-07-15. The listed applicant is Biocircuit Technologies, Incorporated. The 510(k) number is K210665.

When did Nerve Tape receive FDA 510(k) clearance?

Nerve Tape received FDA 510(k) clearance on 2022-07-15, under 510(k) number K210665.

Who is the listed applicant for Nerve Tape?

The FDA 510(k) record lists Biocircuit Technologies, Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nerve Tape?

The FDA product code for Nerve Tape is JXI.

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。

相關器械(代碼:JXI)

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。

↑