FDA 510(k)

FUSION Plus 照明灯

K号: K180065 · 2019-04-19

决定日期2019-04-19

产品代码EBZ

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决定实质等同

器械摘要

FUSION Plus Curing Light is the device name listed in this FDA 510(k) record. The listed applicant is Dentlight, Inc.. It received FDA 510(k) clearance on 2019-04-19 under 510(k) number K180065. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the FUSION Plus Curing Light?

FUSION Plus Curing Light is a medical device that received FDA 510(k) clearance on 2019-04-19. The listed applicant is Dentlight, Inc.. The 510(k) number is K180065.

When did FUSION Plus Curing Light receive FDA 510(k) clearance?

FUSION Plus Curing Light received FDA 510(k) clearance on 2019-04-19, under 510(k) number K180065.

Who is the listed applicant for FUSION Plus Curing Light?

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

What is the FDA product code for FUSION Plus Curing Light?

The FDA product code for FUSION Plus Curing Light is EBZ.

列明Dentlight, Inc.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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