FDA 510(k)

Vitalograph型号2120 In2itive电子日记

K号: K200550 · 2020-07-27

决定日期2020-07-27

产品代码BZG

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决定实质等同

器械摘要

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.

常见问题

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.

列明Vitalograph Ireland, Ltd.为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

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