FDA 510(k)

Tenex Health TX 系統搭配 TXP 微針

K 號：K181367 · 2018-08-28

決定日期2018-08-28

產品代碼LFL

決定相當於

器材摘要

Tenex Health TX System with the TXP MicroTip is the device name listed in this FDA 510(k) record. The listed applicant is Tenex Health, Inc.. It received FDA 510(k) clearance on 2018-08-28 under 510(k) number K181367. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

常見問題

What is the Tenex Health TX System with the TXP MicroTip?

Tenex Health TX System with the TXP MicroTip is a medical device that received FDA 510(k) clearance on 2018-08-28. The listed applicant is Tenex Health, Inc.. The 510(k) number is K181367.

When did Tenex Health TX System with the TXP MicroTip receive FDA 510(k) clearance?

Tenex Health TX System with the TXP MicroTip received FDA 510(k) clearance on 2018-08-28, under 510(k) number K181367.

Who is the listed applicant for Tenex Health TX System with the TXP MicroTip?

The FDA 510(k) record lists Tenex Health, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Tenex Health TX System with the TXP MicroTip?

The FDA product code for Tenex Health TX System with the TXP MicroTip is LFL.

其他以 Tenex Health, Inc. 為申請人之記錄

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K153299Tenex Health TX 系統

相關器械（代碼：LFL）

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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