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FDA 510(k)

Envision 超声垫和盖

K号: K190802 · 2019-05-24

决定日期2019-05-24
产品代码ITX
咨询委员会RA
决定实质等同

器械摘要

Envision ultrasound pad and cover is the device name listed in this FDA 510(k) record. The listed applicant is Civco Medical Solutions. It received FDA 510(k) clearance on 2019-05-24 under 510(k) number K190802. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Envision ultrasound pad and cover?

Envision ultrasound pad and cover is a medical device that received FDA 510(k) clearance on 2019-05-24. The listed applicant is Civco Medical Solutions. The 510(k) number is K190802.

When did Envision ultrasound pad and cover receive FDA 510(k) clearance?

Envision ultrasound pad and cover received FDA 510(k) clearance on 2019-05-24, under 510(k) number K190802.

Who is the listed applicant for Envision ultrasound pad and cover?

The FDA 510(k) record lists Civco Medical Solutions as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Envision ultrasound pad and cover?

The FDA product code for Envision ultrasound pad and cover is ITX.

相关临床试验

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。

列明Civco Medical Solutions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:ITX)

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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