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FDA 510(k)

Sim&Size

K号: K212373 · 2022-01-27

申请人Sim&Cure
决定日期2022-01-27
产品代码PZO
咨询委员会RA
决定实质等同

器械摘要

Sim&Size is the device name listed in this FDA 510(k) record. The listed applicant is Sim&Cure. It received FDA 510(k) clearance on 2022-01-27 under 510(k) number K212373. The device is classified under product code PZO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Sim&Size?

Sim&Size is a medical device that received FDA 510(k) clearance on 2022-01-27. The listed applicant is Sim&Cure. The 510(k) number is K212373.

When did Sim&Size receive FDA 510(k) clearance?

Sim&Size received FDA 510(k) clearance on 2022-01-27, under 510(k) number K212373.

Who is the listed applicant for Sim&Size?

The FDA 510(k) record lists Sim&Cure as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Sim&Size?

The FDA product code for Sim&Size is PZO.

列明Sim&Cure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。

相关器械(代码:PZO)

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。

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。

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