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FDA 510(k)

Tenso TS-101S 及 TS-101D 一次性血壓袖帶

K 號:K153251 · 2016-04-14

決定日期2016-04-14
產品代碼DXQ
諮詢委員會履歷
決定相當於

器材摘要

Tenso TS-101S and TS-101D Disposable Blood Pressure Cuff is the device name listed in this FDA 510(k) record. The listed applicant is Ningbo Free Trade Zone Tenso Medical Instruments Co., Ltd.. It received FDA 510(k) clearance on 2016-04-14 under 510(k) number K153251. The device is classified under product code DXQ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Tenso TS-101S and TS-101D Disposable Blood Pressure Cuff?

Tenso TS-101S and TS-101D Disposable Blood Pressure Cuff is a medical device that received FDA 510(k) clearance on 2016-04-14. The listed applicant is Ningbo Free Trade Zone Tenso Medical Instruments Co., Ltd.. The 510(k) number is K153251.

When did Tenso TS-101S and TS-101D Disposable Blood Pressure Cuff receive FDA 510(k) clearance?

Tenso TS-101S and TS-101D Disposable Blood Pressure Cuff received FDA 510(k) clearance on 2016-04-14, under 510(k) number K153251.

Who is the listed applicant for Tenso TS-101S and TS-101D Disposable Blood Pressure Cuff?

The FDA 510(k) record lists Ningbo Free Trade Zone Tenso Medical Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Tenso TS-101S and TS-101D Disposable Blood Pressure Cuff?

The FDA product code for Tenso TS-101S and TS-101D Disposable Blood Pressure Cuff is DXQ.

相關臨床試驗

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相關器械(代碼:DXQ)

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

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