免责声明: 本站汇总 FDA、ClinicalTrials.gov、PubMed、SEC EDGAR 等官方公开数据,仅供一般参考,不构成医疗建议、诊断、治疗建议或投资建议。

FDA 510(k)

Medisystem PACS

K号: K223048 · 2023-06-23

决定日期2023-06-23
产品代码LLZ
咨询委员会RA
决定实质等同

器械摘要

Medisystem Pacs is the device name listed in this FDA 510(k) record. The listed applicant is Medilab Manutencao E Sitemas Ltda. It received FDA 510(k) clearance on 2023-06-23 under 510(k) number K223048. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Medisystem Pacs?

Medisystem Pacs is a medical device that received FDA 510(k) clearance on 2023-06-23. The listed applicant is Medilab Manutencao E Sitemas Ltda. The 510(k) number is K223048.

When did Medisystem Pacs receive FDA 510(k) clearance?

Medisystem Pacs received FDA 510(k) clearance on 2023-06-23, under 510(k) number K223048.

Who is the listed applicant for Medisystem Pacs?

The FDA 510(k) record lists Medilab Manutencao E Sitemas Ltda as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Medisystem Pacs?

The FDA product code for Medisystem Pacs is LLZ.

相关临床试验

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:LLZ)

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。

↑