FDA 510(k)

维斯塔清晰

K号: K193389 · 2020-03-04

决定日期2020-03-04

产品代码MVL

决定实质等同

器械摘要

Vista Clear 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 2020-03-04 under 510(k) number K193389. The device is classified under product code MVL. FDA Decision: Substantially Equivalent.

常见问题

What is the Vista Clear?

Vista Clear is a medical device that received FDA 510(k) clearance on 2020-03-04. The listed applicant is Inter-Med/Vista Dental Products. The 510(k) number is K193389.

When did Vista Clear receive FDA 510(k) clearance?

Vista Clear received FDA 510(k) clearance on 2020-03-04, under 510(k) number K193389.

Who is the listed applicant for Vista Clear?

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 Clear?

The FDA product code for Vista Clear 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。

K193357V-Mix K193409维斯塔冲洗，维斯塔冲洗加强版 K193447维斯塔染料 K190220维斯塔FS，维斯塔FS液体 K170101勇敢固化灯

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。