FDA 510(k)

Precision DL

K号: K223212 · 2023-04-27

决定日期2023-04-27

产品代码KPS

咨询委员会RA

决定实质等同

器械摘要

Precision DL is the device name listed in this FDA 510(k) record. The listed applicant is GE Healthcare. It received FDA 510(k) clearance on 2023-04-27 under 510(k) number K223212. The device is classified under product code KPS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Precision DL?

Precision DL is a medical device that received FDA 510(k) clearance on 2023-04-27. The listed applicant is GE Healthcare. The 510(k) number is K223212.

When did Precision DL receive FDA 510(k) clearance?

Precision DL received FDA 510(k) clearance on 2023-04-27, under 510(k) number K223212.

Who is the listed applicant for Precision DL?

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

What is the FDA product code for Precision DL?

The FDA product code for Precision DL is KPS.

列明GE Healthcare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。

K253639查看此医疗设备监管文本： View the medical-device regulatory text for this device_name.K242925MR Contour DL K232346数字专家访问与远程扫描 K221680Xeleris V 处理与审查系统 K221932Omni 传奇 K213689Voluson P6，Voluson P8

查看所有 55 个设备 →

相关器械（代码：KPS）

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。