中风和 CPAP 结果研究 3 随机对照试验
K号: K152584 · 2016-01-20
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器械摘要
Stroke VCAR is the device name listed in this FDA 510(k) record. The listed applicant is GE Medical Systems SCS. It received FDA 510(k) clearance on 2016-01-20 under 510(k) number K152584. The device is classified under product code JAK. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Stroke VCAR?
Stroke VCAR is a medical device that received FDA 510(k) clearance on 2016-01-20. The listed applicant is GE Medical Systems SCS. The 510(k) number is K152584.
When did Stroke VCAR receive FDA 510(k) clearance?
Stroke VCAR received FDA 510(k) clearance on 2016-01-20, under 510(k) number K152584.
Who is the listed applicant for Stroke VCAR?
FDA 510(k)记录列出了GE医疗系统SCS为申请人。这本身并不能确立该设备制造商。
What is the FDA product code for Stroke VCAR?
The FDA product code for Stroke VCAR is JAK.
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GE Medical Systems SCS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。
相关器械（代码：JAK）
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。
K261125BodyTom 64（NL4100）；OmniTom Elite（NL5000）Samsung HME America, Inc., dba NeuroLogica Corp.K261229SCENARIA 视觉阶段 6.0Fujifilm CorporationK253836FCT iStream 阶段 2Fujifilm CorporationK253450BodyTom Elite (NL4000)NeuroLogica Corp., a Samsung CompanyK253770CardIQ 套件GE Medical Systems SCSK253560Enhanced Boundary for PCCTGe Medical Systems, 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。
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