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)

FloTrac 传感器;FloTrac Jr 传感器;Acumen IQ 传感器;VolumeView 传感器

K号: K242909 · 2025-03-21

决定日期2025-03-21
产品代码DRS
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

FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensors is the device name listed in this FDA 510(k) record. The listed applicant is Edwards Lifesciences, LLC. It received FDA 510(k) clearance on 2025-03-21 under 510(k) number K242909. The device is classified under product code DRS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensors?

FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensors is a medical device that received FDA 510(k) clearance on 2025-03-21. The listed applicant is Edwards Lifesciences, LLC. The 510(k) number is K242909.

When did FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensors receive FDA 510(k) clearance?

FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensors received FDA 510(k) clearance on 2025-03-21, under 510(k) number K242909.

Who is the listed applicant for FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensors?

The FDA 510(k) record lists Edwards Lifesciences, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensors?

The FDA product code for FloTrac sensors; FloTrac Jr sensors; Acumen IQ sensors; VolumeView sensors is DRS.

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。

列明Edwards Lifesciences, LLC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。

查看所有 53 个设备 →

相关器械(代码:DRS)

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。

↑