FDA 510(k)

Vitalograph 模型 2120 In2itive 電子日記

K 號：K200550 · 2020-07-27

決定日期2020-07-27

產品代碼BZG

諮詢委員會AN

決定相當於

器材摘要

Vitalograph Model 2120 In2itive eDiary is the device name listed in this FDA 510(k) record. The listed applicant is Vitalograph Ireland, Ltd.. It received FDA 510(k) clearance on 2020-07-27 under 510(k) number K200550. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Vitalograph Model 2120 In2itive eDiary?

Vitalograph Model 2120 In2itive eDiary is a medical device that received FDA 510(k) clearance on 2020-07-27. The listed applicant is Vitalograph Ireland, Ltd.. The 510(k) number is K200550.

When did Vitalograph Model 2120 In2itive eDiary receive FDA 510(k) clearance?

Vitalograph Model 2120 In2itive eDiary received FDA 510(k) clearance on 2020-07-27, under 510(k) number K200550.

Who is the listed applicant for Vitalograph Model 2120 In2itive eDiary?

The FDA 510(k) record lists Vitalograph Ireland, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vitalograph Model 2120 In2itive eDiary?

The FDA product code for Vitalograph Model 2120 In2itive eDiary is BZG.

其他以 Vitalograph Ireland, Ltd. 為申請人之記錄

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