FDA 510(k)

MESI mTablet ECG诊断系统，MESI mTablet ECG

K号: K223670 · 2023-07-28

申请人Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O.

决定日期2023-07-28

产品代码DPS

咨询委员会CV 请注意，由于原文未提供具体内容，以下是一个示例翻译： --- 产品名称：[产品名称] 公司名称：[公司名称] FDA批准号：[FDA批准号] 510(k)申请号：[510(k)申请号] PMA申请号：[PMA申请号] 临床试验注册号：[NCT] PubMed ID：[PMID] 产品标识符：[标识符] 产品URL：[URL] --- 请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。

决定实质等同

器械摘要

MESI mTablet ECG Diagnostic System, MESI mTablet ECG is the device name listed in this FDA 510(k) record. The listed applicant is Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O.. It received FDA 510(k) clearance on 2023-07-28 under 510(k) number K223670. The device is classified under product code DPS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the MESI mTablet ECG Diagnostic System, MESI mTablet ECG?

MESI mTablet ECG Diagnostic System, MESI mTablet ECG is a medical device that received FDA 510(k) clearance on 2023-07-28. The listed applicant is Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O.. The 510(k) number is K223670.

When did MESI mTablet ECG Diagnostic System, MESI mTablet ECG receive FDA 510(k) clearance?

MESI mTablet ECG Diagnostic System, MESI mTablet ECG received FDA 510(k) clearance on 2023-07-28, under 510(k) number K223670.

Who is the listed applicant for MESI mTablet ECG Diagnostic System, MESI mTablet ECG?

The FDA 510(k) record lists Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MESI mTablet ECG Diagnostic System, MESI mTablet ECG?

The FDA product code for MESI mTablet ECG Diagnostic System, MESI mTablet ECG is DPS.

列明Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O.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。

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