FDA 510(k)

维斯塔FS，维斯塔FS液体

K号: K190220 · 2019-06-10

决定日期2019-06-10

产品代码MVL

决定实质等同

器械摘要

Vista FS, Vista FS Liquid is the device name listed in this FDA 510(k) record. The listed applicant is Inter-Med/Vista Dental Products. It received FDA 510(k) clearance on 2019-06-10 under 510(k) number K190220. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.

常见问题

What is the Vista FS, Vista FS Liquid?

Vista FS, Vista FS Liquid is a medical device that received FDA 510(k) clearance on 2019-06-10. The listed applicant is Inter-Med/Vista Dental Products. The 510(k) number is K190220.

When did Vista FS, Vista FS Liquid receive FDA 510(k) clearance?

Vista FS, Vista FS Liquid received FDA 510(k) clearance on 2019-06-10, under 510(k) number K190220.

Who is the listed applicant for Vista FS, Vista FS Liquid?

The FDA 510(k) record lists Inter-Med/Vista Dental Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vista FS, Vista FS Liquid?

The FDA product code for Vista FS, Vista FS Liquid is MVL.

列明Inter-Med/Vista Dental Products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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