FDA 510(k)

MMPC-4127F1

K号: K172922 · 2017-12-21

决定日期2017-12-21

产品代码PZZ

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决定实质等同

器械摘要

MMPC-4127F1 is the device name listed in this FDA 510(k) record. The listed applicant is Barco N.V.. It received FDA 510(k) clearance on 2017-12-21 under 510(k) number K172922. The device is classified under product code PZZ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the MMPC-4127F1?

MMPC-4127F1 is a medical device that received FDA 510(k) clearance on 2017-12-21. The listed applicant is Barco N.V.. The 510(k) number is K172922.

When did MMPC-4127F1 receive FDA 510(k) clearance?

MMPC-4127F1 received FDA 510(k) clearance on 2017-12-21, under 510(k) number K172922.

Who is the listed applicant for MMPC-4127F1?

The FDA 510(k) record lists Barco N.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MMPC-4127F1?

The FDA product code for MMPC-4127F1 is PZZ.

列明Barco N.V.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。

K243307LCD 显示器 (MDEC-2523)K242008Coronis OneLook K233693Nio Color 8MP（MDNC-8132）K230520Nio Color 2MP（MDNC-2521）；Nio Color 3MP（MDNC-3521）K213957Demetra Dermatoscope BDEM-01 K203364MDPC-8127

查看所有 18 个设备 →

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。

器械摘要

常见问题

列明Barco N.V.为申报人的其他记录

相关器械（代码：PZZ）

官方来源