FDA 510(k)

BP-BT 選擇機

K 號：K200287 · 2020-05-15

決定日期2020-05-15

產品代碼DXN

諮詢委員會履歷

決定相當於

器材摘要

BP-BT Kiosk is the device name listed in this FDA 510(k) record. The listed applicant is Ld Technology, LLC. It received FDA 510(k) clearance on 2020-05-15 under 510(k) number K200287. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the BP-BT Kiosk?

BP-BT Kiosk is a medical device that received FDA 510(k) clearance on 2020-05-15. The listed applicant is Ld Technology, LLC. The 510(k) number is K200287.

When did BP-BT Kiosk receive FDA 510(k) clearance?

BP-BT Kiosk received FDA 510(k) clearance on 2020-05-15, under 510(k) number K200287.

Who is the listed applicant for BP-BT Kiosk?

The FDA 510(k) record lists Ld Technology, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BP-BT Kiosk?

The FDA product code for BP-BT Kiosk is DXN.

其他以 Ld Technology, LLC 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。

K200141氧氣-W系統 K173696TBL-ABI 系統 K160956LD-Oxi系統

相關器械（代碼：DXN）

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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