FDA 510(k)

CMO8 成人 PMP 氧合器带管路包（型号：CME40009）

K号: K231414 · 2023-11-01

决定日期2023-11-01

产品代码DTZ

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

CMO8 Adult PMP Oxygenator with Tubing Pack (Model: CME40009) is the device name listed in this FDA 510(k) record. The listed applicant is Chalice Medical , Ltd.. It received FDA 510(k) clearance on 2023-11-01 under 510(k) number K231414. The device is classified under product code DTZ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the CMO8 Adult PMP Oxygenator with Tubing Pack (Model: CME40009)?

CMO8 Adult PMP Oxygenator with Tubing Pack (Model: CME40009) is a medical device that received FDA 510(k) clearance on 2023-11-01. The listed applicant is Chalice Medical , Ltd.. The 510(k) number is K231414.

When did CMO8 Adult PMP Oxygenator with Tubing Pack (Model: CME40009) receive FDA 510(k) clearance?

CMO8 Adult PMP Oxygenator with Tubing Pack (Model: CME40009) received FDA 510(k) clearance on 2023-11-01, under 510(k) number K231414.

Who is the listed applicant for CMO8 Adult PMP Oxygenator with Tubing Pack (Model: CME40009)?

The FDA 510(k) record lists Chalice Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CMO8 Adult PMP Oxygenator with Tubing Pack (Model: CME40009)?

The FDA product code for CMO8 Adult PMP Oxygenator with Tubing Pack (Model: CME40009) is DTZ.

列明Chalice Medical , Ltd.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。

K201642Paragon 成人Maxi PMP 氧合器带管包 K191246Paragon 成人Maxi PMP 氧合器（型号：XCMOP405PMP）

相关器械（代码：DTZ）

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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官方来源

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