FDA 510(k)

VSP系统

K号: K192192 · 2020-02-26

决定日期2020-02-26

产品代码DZJ

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决定实质等同

器械摘要

VSP System is the device name listed in this FDA 510(k) record. The listed applicant is 3D Systems. It received FDA 510(k) clearance on 2020-02-26 under 510(k) number K192192. The device is classified under product code DZJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the VSP System?

VSP System is a medical device that received FDA 510(k) clearance on 2020-02-26. The listed applicant is 3D Systems. The 510(k) number is K192192.

When did VSP System receive FDA 510(k) clearance?

VSP System received FDA 510(k) clearance on 2020-02-26, under 510(k) number K192192.

Who is the listed applicant for VSP System?

The FDA 510(k) record lists 3D Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VSP System?

The FDA product code for VSP System is DZJ.

列明3D Systems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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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。