FDA 510(k)

SMART FINDER

K号: K203509 · 2021-07-14

决定日期2021-07-14

产品代码IZH

咨询委员会RA

决定实质等同

器械摘要

SMART FINDER is the device name listed in this FDA 510(k) record. The listed applicant is Ims Giotto S.P.A.. It received FDA 510(k) clearance on 2021-07-14 under 510(k) number K203509. The device is classified under product code IZH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the SMART FINDER?

SMART FINDER is a medical device that received FDA 510(k) clearance on 2021-07-14. The listed applicant is Ims Giotto S.P.A.. The 510(k) number is K203509.

When did SMART FINDER receive FDA 510(k) clearance?

SMART FINDER received FDA 510(k) clearance on 2021-07-14, under 510(k) number K203509.

Who is the listed applicant for SMART FINDER?

The FDA 510(k) record lists Ims Giotto S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SMART FINDER?

The FDA product code for SMART FINDER is IZH.

列明Ims Giotto S.P.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。

K200424Giotto 类（型号 - 3000X-YY 和 4000X-YY）

官方来源

在 FDA 数据库中查看 →

数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。