FDA 510(k)

Swiss LthoClast Trilogy

K号: K230893 · 2023-10-23

决定日期2023-10-23

产品代码FEO

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决定实质等同

器械摘要

Swiss LthoClast Trilogy is the device name listed in this FDA 510(k) record. The listed applicant is E.M.S Electro Medical Systems S.A. It received FDA 510(k) clearance on 2023-10-23 under 510(k) number K230893. The device is classified under product code FEO. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Swiss LthoClast Trilogy?

Swiss LthoClast Trilogy is a medical device that received FDA 510(k) clearance on 2023-10-23. The listed applicant is E.M.S Electro Medical Systems S.A. The 510(k) number is K230893.

When did Swiss LthoClast Trilogy receive FDA 510(k) clearance?

Swiss LthoClast Trilogy received FDA 510(k) clearance on 2023-10-23, under 510(k) number K230893.

Who is the listed applicant for Swiss LthoClast Trilogy?

The FDA 510(k) record lists E.M.S Electro Medical Systems S.A as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Swiss LthoClast Trilogy?

The FDA product code for Swiss LthoClast Trilogy is FEO.

列明E.M.S Electro Medical Systems S.A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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