FDA 510(k)

Veri夹板

K号: K190107 · 2019-07-10

决定日期2019-07-10

产品代码MQC

决定实质等同

器械摘要

VeriSplint is the device name listed in this FDA 510(k) record. The listed applicant is Whip Mix Corporation. It received FDA 510(k) clearance on 2019-07-10 under 510(k) number K190107. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

常见问题

What is the VeriSplint?

VeriSplint is a medical device that received FDA 510(k) clearance on 2019-07-10. The listed applicant is Whip Mix Corporation. The 510(k) number is K190107.

When did VeriSplint receive FDA 510(k) clearance?

VeriSplint received FDA 510(k) clearance on 2019-07-10, under 510(k) number K190107.

Who is the listed applicant for VeriSplint?

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

What is the FDA product code for VeriSplint?

The FDA product code for VeriSplint is MQC.

列明Whip Mix Corporation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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官方来源

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