FDA 510(k)

VTRUST生命徵象監測儀，型號：TD-2300；FORA生命徵象監測儀，型號：VSM100

K 號：K172221 · 2018-06-06

決定日期2018-06-06

產品代碼MWI

諮詢委員會履歷

決定相當於

器材摘要

VTRUST Vital Signs Monitor, Model: TD-2300; FORA Vital Signs Monitor, Model: VSM100 is the device name listed in this FDA 510(k) record. The listed applicant is Taidoc Technology Corporation. It received FDA 510(k) clearance on 2018-06-06 under 510(k) number K172221. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the VTRUST Vital Signs Monitor, Model: TD-2300; FORA Vital Signs Monitor, Model: VSM100?

VTRUST Vital Signs Monitor, Model: TD-2300; FORA Vital Signs Monitor, Model: VSM100 is a medical device that received FDA 510(k) clearance on 2018-06-06. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K172221.

When did VTRUST Vital Signs Monitor, Model: TD-2300; FORA Vital Signs Monitor, Model: VSM100 receive FDA 510(k) clearance?

VTRUST Vital Signs Monitor, Model: TD-2300; FORA Vital Signs Monitor, Model: VSM100 received FDA 510(k) clearance on 2018-06-06, under 510(k) number K172221.

Who is the listed applicant for VTRUST Vital Signs Monitor, Model: TD-2300; FORA Vital Signs Monitor, Model: VSM100?

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

What is the FDA product code for VTRUST Vital Signs Monitor, Model: TD-2300; FORA Vital Signs Monitor, Model: VSM100?

The FDA product code for VTRUST Vital Signs Monitor, Model: TD-2300; FORA Vital Signs Monitor, Model: VSM100 is MWI.

其他以 Taidoc Technology Corporation 為申請人之記錄

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相關器械（代碼：MWI）

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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