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)

HyperView高光谱组织氧合测量系统

K号: K161237 · 2016-12-16

决定日期2016-12-16
产品代码MUD
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

HyperView Hyperspectral Tissue Oxygenation Measurement System is the device name listed in this FDA 510(k) record. The listed applicant is Hypermed Imaging, Inc.. It received FDA 510(k) clearance on 2016-12-16 under 510(k) number K161237. The device is classified under product code MUD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the HyperView Hyperspectral Tissue Oxygenation Measurement System?

HyperView Hyperspectral Tissue Oxygenation Measurement System is a medical device that received FDA 510(k) clearance on 2016-12-16. The listed applicant is Hypermed Imaging, Inc.. The 510(k) number is K161237.

When did HyperView Hyperspectral Tissue Oxygenation Measurement System receive FDA 510(k) clearance?

HyperView Hyperspectral Tissue Oxygenation Measurement System received FDA 510(k) clearance on 2016-12-16, under 510(k) number K161237.

Who is the listed applicant for HyperView Hyperspectral Tissue Oxygenation Measurement System?

The FDA 510(k) record lists Hypermed Imaging, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HyperView Hyperspectral Tissue Oxygenation Measurement System?

The FDA product code for HyperView Hyperspectral Tissue Oxygenation Measurement System is MUD.

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:MUD)

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。

↑