FDA 510(k)

Fusion Bond 5, Fusion Bond 7, Fusion Bond DC, Renew MDP, Renew Universal

K号: K231696 · 2023-08-11

决定日期2023-08-11

产品代码KLE

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决定实质等同

器械摘要

Fusion Bond 5, Fusion Bond 7, Fusion Bond DC, Renew MDP, Renew Universal is the device name listed in this FDA 510(k) record. The listed applicant is Prevest Denpro Limited. It received FDA 510(k) clearance on 2023-08-11 under 510(k) number K231696. The device is classified under product code KLE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Fusion Bond 5, Fusion Bond 7, Fusion Bond DC, Renew MDP, Renew Universal?

Fusion Bond 5, Fusion Bond 7, Fusion Bond DC, Renew MDP, Renew Universal is a medical device that received FDA 510(k) clearance on 2023-08-11. The listed applicant is Prevest Denpro Limited. The 510(k) number is K231696.

When did Fusion Bond 5, Fusion Bond 7, Fusion Bond DC, Renew MDP, Renew Universal receive FDA 510(k) clearance?

Fusion Bond 5, Fusion Bond 7, Fusion Bond DC, Renew MDP, Renew Universal received FDA 510(k) clearance on 2023-08-11, under 510(k) number K231696.

Who is the listed applicant for Fusion Bond 5, Fusion Bond 7, Fusion Bond DC, Renew MDP, Renew Universal?

The FDA 510(k) record lists Prevest Denpro Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Fusion Bond 5, Fusion Bond 7, Fusion Bond DC, Renew MDP, Renew Universal?

The FDA product code for Fusion Bond 5, Fusion Bond 7, Fusion Bond DC, Renew MDP, Renew Universal is KLE.

列明Prevest Denpro Limited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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官方来源

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