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)

Tenax激光抗性气管插管

K号: K213028 · 2021-10-21

决定日期2021-10-21
产品代码BTR
咨询委员会AN 请注意,由于您没有提供完整的医疗设备监管文本,我无法提供完整的翻译。如果您能提供完整的文本,我将很乐意为您翻译。
决定实质等同

器械摘要

Tenax Laser Resistant Endotracheal Tube is the device name listed in this FDA 510(k) record. The listed applicant is Bryan Medical, Inc.. It received FDA 510(k) clearance on 2021-10-21 under 510(k) number K213028. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the Tenax Laser Resistant Endotracheal Tube?

Tenax Laser Resistant Endotracheal Tube is a medical device that received FDA 510(k) clearance on 2021-10-21. The listed applicant is Bryan Medical, Inc.. The 510(k) number is K213028.

When did Tenax Laser Resistant Endotracheal Tube receive FDA 510(k) clearance?

Tenax Laser Resistant Endotracheal Tube received FDA 510(k) clearance on 2021-10-21, under 510(k) number K213028.

Who is the listed applicant for Tenax Laser Resistant Endotracheal Tube?

FDA 510(k)记录显示,Bryan Medical, Inc.为申请人。这本身并不能确立该设备制造商的身份。

What is the FDA product code for Tenax Laser Resistant Endotracheal Tube?

The FDA product code for Tenax Laser Resistant Endotracheal Tube is BTR.

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Bryan Medical, Inc.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:BTR)

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。

↑