FDA 510(k)

BEED 2,5, BEED 3,8

K号: K233002 · 2024-03-20

决定日期2024-03-20

产品代码GEI

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决定实质等同

器械摘要

BEED 2,5, BEED 3,8 is the device name listed in this FDA 510(k) record. The listed applicant is Excelsior Resources, LLC. It received FDA 510(k) clearance on 2024-03-20 under 510(k) number K233002. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BEED 2,5, BEED 3,8?

BEED 2,5, BEED 3,8 is a medical device that received FDA 510(k) clearance on 2024-03-20. The listed applicant is Excelsior Resources, LLC. The 510(k) number is K233002.

When did BEED 2,5, BEED 3,8 receive FDA 510(k) clearance?

BEED 2,5, BEED 3,8 received FDA 510(k) clearance on 2024-03-20, under 510(k) number K233002.

Who is the listed applicant for BEED 2,5, BEED 3,8?

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

What is the FDA product code for BEED 2,5, BEED 3,8?

The FDA product code for BEED 2,5, BEED 3,8 is GEI.

相关器械（代码：GEI）

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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