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FDA 510(k)

EVA15

K号: K202799 · 2020-10-21

决定日期2020-10-21
产品代码HIF
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决定实质等同

器械摘要

EVA15 is the device name listed in this FDA 510(k) record. The listed applicant is Palliare , Ltd.. It received FDA 510(k) clearance on 2020-10-21 under 510(k) number K202799. The device is classified under product code HIF. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the EVA15?

EVA15 is a medical device that received FDA 510(k) clearance on 2020-10-21. The listed applicant is Palliare , Ltd.. The 510(k) number is K202799.

When did EVA15 receive FDA 510(k) clearance?

EVA15 received FDA 510(k) clearance on 2020-10-21, under 510(k) number K202799.

Who is the listed applicant for EVA15?

The FDA 510(k) record lists Palliare , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EVA15?

The FDA product code for EVA15 is HIF.

列明Palliare , 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。

相关器械(代码:HIF)

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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