INSPIRA ART100
K号: K232788 · 2024-05-24
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决定日期2024-05-24
产品代码DWA
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：
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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]
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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
INSPIRA ART100 is the device name listed in this FDA 510(k) record. The listed applicant is Inspira Technologies Oxy B.H.N. , Ltd.. It received FDA 510(k) clearance on 2024-05-24 under 510(k) number K232788. The device is classified under product code DWA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the INSPIRA ART100?
INSPIRA ART100 is a medical device that received FDA 510(k) clearance on 2024-05-24. The listed applicant is Inspira Technologies Oxy B.H.N. , Ltd.. The 510(k) number is K232788.
When did INSPIRA ART100 receive FDA 510(k) clearance?
INSPIRA ART100 received FDA 510(k) clearance on 2024-05-24, under 510(k) number K232788.
Who is the listed applicant for INSPIRA ART100?
The FDA 510(k) record lists Inspira Technologies Oxy B.H.N. , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INSPIRA ART100?
The FDA product code for INSPIRA ART100 is DWA.
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：DWA）
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。
K230698Anivia SG1000 Pump ConsoleApmtd, Inc.K221491Anivia SG1000 Pump ConsoleApmtd, Inc.K192838Quantumn 中心血泵驱动-高压, Quantumn 中心血泵驱动-中压Spectrum Medical , Ltd.K200306CentriMag循环支持系统，CentriMag回（动脉）导管套装，CentriMag引流（静脉）导管套装Abbott (Formerly Thoratec Corporation)K191557CentriMag急性循环支持系统Thoratec Corporation (Now Part of Abbott)
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。
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