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FDA 510(k)

ADVIA Centaur 胰岛素（IRI）主曲线材料（MCM），ADVIA Centaur（IRI）校准器

K号: K162538 · 2016-11-17

申请人Siemens Healthcare Diagnostics
决定日期2016-11-17
产品代码JIT
咨询委员会CH 请注意，您提供的文本“CH”不足以进行翻译。请提供完整的医疗设备监管文本，以便我能够进行准确的翻译。
决定实质等同

器械摘要

ADVIA Centaur Insulin (IRI) Master Curve Material (MCM), ADVIA Centaur (IRI) Calibrator is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Healthcare Diagnostics. It received FDA 510(k) clearance on 2016-11-17 under 510(k) number K162538. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ADVIA Centaur Insulin (IRI) Master Curve Material (MCM), ADVIA Centaur (IRI) Calibrator?

ADVIA Centaur Insulin (IRI) Master Curve Material (MCM), ADVIA Centaur (IRI) Calibrator is a medical device that received FDA 510(k) clearance on 2016-11-17. The listed applicant is Siemens Healthcare Diagnostics. The 510(k) number is K162538.

When did ADVIA Centaur Insulin (IRI) Master Curve Material (MCM), ADVIA Centaur (IRI) Calibrator receive FDA 510(k) clearance?

ADVIA Centaur Insulin (IRI) Master Curve Material (MCM), ADVIA Centaur (IRI) Calibrator received FDA 510(k) clearance on 2016-11-17, under 510(k) number K162538.

Who is the listed applicant for ADVIA Centaur Insulin (IRI) Master Curve Material (MCM), ADVIA Centaur (IRI) Calibrator?

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

What is the FDA product code for ADVIA Centaur Insulin (IRI) Master Curve Material (MCM), ADVIA Centaur (IRI) Calibrator?

The FDA product code for ADVIA Centaur Insulin (IRI) Master Curve Material (MCM), ADVIA Centaur (IRI) Calibrator is JIT.

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

列明Siemens Healthcare Diagnostics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。

K243570Dimension LOCI促甲状腺激素灵活试剂盒（TSHL）；Dimension LOCI游离甲状腺素灵活试剂盒（FT4L）K162977ADVIA 2120i, ADVIA 2120K162298LOCI 总维生素D总测定，LOCI VITD CALK161954Atellica Solution, Atellica A-LYTE 集成多传感器 Na+/K+/CI-, Atellica CH 白蛋白BCP试剂 (Alb_p), Atellica IM 促甲状腺激素 TSH, Atellica CH 万古霉素 (Vanc)K151964Xprecia Stride 凝血系统，Xprecia 系统 PT 控制

相关器械（代码：JIT）

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。

K171168VITROS 免疫诊断产品 胰岛素校准器Ortho Clinical DiagnosticsK170938CalSet IGF-1Roche DiagnosticsK170160Abbott ARCHITECT Free T3Abbott LaboratoriesK163546Lumipulse G 孕酮-N 校准器Fujirebio Diagnostics,Inc.K163534Lumipulse G FSH-N 校准器Fujirebio Diagnostics,Inc.K163544Lumipulse G 乳糜素Fujirebio Diagnostics,Inc.

官方来源

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