FDA 510(k)

Game Ready GRPro 2.1 系统

K号: K192114 · 2019-10-29

决定日期2019-10-29

产品代码IRP

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决定实质等同

器械摘要

Game Ready GRPro 2.1 System is the device name listed in this FDA 510(k) record. The listed applicant is Cool Systems, Inc. (Dba Game Ready). It received FDA 510(k) clearance on 2019-10-29 under 510(k) number K192114. The device is classified under product code IRP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Game Ready GRPro 2.1 System?

Game Ready GRPro 2.1 System is a medical device that received FDA 510(k) clearance on 2019-10-29. The listed applicant is Cool Systems, Inc. (Dba Game Ready). The 510(k) number is K192114.

When did Game Ready GRPro 2.1 System receive FDA 510(k) clearance?

Game Ready GRPro 2.1 System received FDA 510(k) clearance on 2019-10-29, under 510(k) number K192114.

Who is the listed applicant for Game Ready GRPro 2.1 System?

The FDA 510(k) record lists Cool Systems, Inc. (Dba Game Ready) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Game Ready GRPro 2.1 System?

The FDA product code for Game Ready GRPro 2.1 System is IRP.

列明Cool Systems, Inc. (Dba Game Ready)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。

K171685Med4 Elite

相关器械（代码：IRP）

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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