FDA 510(k)

Dentca Denture Base II

K号: K162044 · 2017-03-03

决定日期2017-03-03

产品代码EBI

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决定实质等同

器械摘要

Dentca Denture Base II is the device name listed in this FDA 510(k) record. The listed applicant is Dentca, Inc.. It received FDA 510(k) clearance on 2017-03-03 under 510(k) number K162044. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Dentca Denture Base II?

Dentca Denture Base II is a medical device that received FDA 510(k) clearance on 2017-03-03. The listed applicant is Dentca, Inc.. The 510(k) number is K162044.

When did Dentca Denture Base II receive FDA 510(k) clearance?

Dentca Denture Base II received FDA 510(k) clearance on 2017-03-03, under 510(k) number K162044.

Who is the listed applicant for Dentca Denture Base II?

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

What is the FDA product code for Dentca Denture Base II?

The FDA product code for Dentca Denture Base II is EBI.

列明Dentca, 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。

K261474DENTCA Tru Flexible K220042Dentca Base Premium，Dentca Base Hi-Impact K192806DENTCA 冠桥 K172398DENTCA 假牙牙齿

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