TunnelVision 内窥镜软组织松解系统及 HBL 刀具组件
K号: K252020 · 2025-10-15
广告
器械摘要
常见问题
What is the TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly?
TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly is a medical device that received FDA 510(k) clearance on 2025-10-15. The listed applicant is Hand Biomechanics Lab, Inc.. The 510(k) number is K252020.
When did TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly receive FDA 510(k) clearance?
TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly received FDA 510(k) clearance on 2025-10-15, under 510(k) number K252020.
Who is the listed applicant for TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly?
The FDA 510(k) record lists Hand Biomechanics Lab, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly?
The FDA product code for TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly is HRX.
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Hand Biomechanics Lab, 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:HRX)
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。
广告