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FDA 510(k)

DR 100s

K号: K191884 · 2019-08-09

申请人Agfa N.V.
决定日期2019-08-09
产品代码IZL
咨询委员会RA
决定实质等同

器械摘要

DR 100s is the device name listed in this FDA 510(k) record. The listed applicant is Agfa N.V.. It received FDA 510(k) clearance on 2019-08-09 under 510(k) number K191884. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the DR 100s?

DR 100s is a medical device that received FDA 510(k) clearance on 2019-08-09. The listed applicant is Agfa N.V.. The 510(k) number is K191884.

When did DR 100s receive FDA 510(k) clearance?

DR 100s received FDA 510(k) clearance on 2019-08-09, under 510(k) number K191884.

Who is the listed applicant for DR 100s?

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

What is the FDA product code for DR 100s?

The FDA product code for DR 100s is IZL.

列明Agfa 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。

相关器械(代码:IZL)

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。

官方来源

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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。

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