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)

HemoSphere高级监测仪，取景器遥控器，HemoSphere高级监测平台

K号: K211465 · 2021-07-08

申请人Edwards Lfesciences
决定日期2021-07-08
产品代码DQK
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

HemoSphere Advanced Monitor, Viewfinder Remote, HemoSphere Advanced Monitoring Platform is the device name listed in this FDA 510(k) record. The listed applicant is Edwards Lfesciences. It received FDA 510(k) clearance on 2021-07-08 under 510(k) number K211465. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the HemoSphere Advanced Monitor, Viewfinder Remote, HemoSphere Advanced Monitoring Platform?

HemoSphere Advanced Monitor, Viewfinder Remote, HemoSphere Advanced Monitoring Platform is a medical device that received FDA 510(k) clearance on 2021-07-08. The listed applicant is Edwards Lfesciences. The 510(k) number is K211465.

When did HemoSphere Advanced Monitor, Viewfinder Remote, HemoSphere Advanced Monitoring Platform receive FDA 510(k) clearance?

HemoSphere Advanced Monitor, Viewfinder Remote, HemoSphere Advanced Monitoring Platform received FDA 510(k) clearance on 2021-07-08, under 510(k) number K211465.

Who is the listed applicant for HemoSphere Advanced Monitor, Viewfinder Remote, HemoSphere Advanced Monitoring Platform?

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

What is the FDA product code for HemoSphere Advanced Monitor, Viewfinder Remote, HemoSphere Advanced Monitoring Platform?

The FDA product code for HemoSphere Advanced Monitor, Viewfinder Remote, HemoSphere Advanced Monitoring Platform is DQK.

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。

NCT07608549FLASHPilot 1期安全性研究NOT_YET_RECRUITINGNCT06562205PAP系统外部临床研究（ECS）NOT_YET_RECRUITINGNCT06443177交感神经调节对动脉瘤性蛛网膜下腔出血继发脑动脉痉挛的影响SUSPENDEDNCT07095751人工智能辅助尿路摄像头评估系统，用于诊断膀胱癌NOT_YET_RECRUITING

相关器械（代码：DQK）

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。

K261729EnSite™ X EP系统Abbott MedicalK262005Affera 集成映射系统Medtronic, Inc.K253692AVVIGO™+ 多模态引导系统Boston ScientificK253576CorVista系统®带PCWP附加组件Analytics For Life, Inc.K262006EnSite™ X EP系统Abbott MedicalK252978ScioCardio心电图分析平台Synergen Technology Labs, LLC

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。

↑