FDA 510(k)

Upcera 釉料膏，釉料粉，和釉料液体

K号: K181167 · 2018-09-02

决定日期2018-09-02

产品代码EIH

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决定实质等同

器械摘要

Upcera Glaze Paste, Glaze Powder, and Glaze Liquid is the device name listed in this FDA 510(k) record. The listed applicant is Liaoning Upcera Co., Ltd.. It received FDA 510(k) clearance on 2018-09-02 under 510(k) number K181167. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Upcera Glaze Paste, Glaze Powder, and Glaze Liquid?

Upcera Glaze Paste, Glaze Powder, and Glaze Liquid is a medical device that received FDA 510(k) clearance on 2018-09-02. The listed applicant is Liaoning Upcera Co., Ltd.. The 510(k) number is K181167.

When did Upcera Glaze Paste, Glaze Powder, and Glaze Liquid receive FDA 510(k) clearance?

Upcera Glaze Paste, Glaze Powder, and Glaze Liquid received FDA 510(k) clearance on 2018-09-02, under 510(k) number K181167.

Who is the listed applicant for Upcera Glaze Paste, Glaze Powder, and Glaze Liquid?

The FDA 510(k) record lists Liaoning Upcera Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Upcera Glaze Paste, Glaze Powder, and Glaze Liquid?

The FDA product code for Upcera Glaze Paste, Glaze Powder, and Glaze Liquid is EIH.

列明Liaoning Upcera Co., Ltd.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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