手动组织移除装置
K号: K254050 · 2026-05-15
广告
器械摘要
常见问题
What is the Manual Tissue Removal Device?
Manual Tissue Removal Device is a medical device that received FDA 510(k) clearance on 2026-05-15. The listed applicant is Suzhou AcuVu Medical Technology Co., Ltd.. The 510(k) number is K254050.
When did Manual Tissue Removal Device receive FDA 510(k) clearance?
Manual Tissue Removal Device received FDA 510(k) clearance on 2026-05-15, under 510(k) number K254050.
Who is the listed applicant for Manual Tissue Removal Device?
The FDA 510(k) record lists Suzhou AcuVu Medical Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Manual Tissue Removal Device?
The FDA product code for Manual Tissue Removal Device is HIH.
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Suzhou AcuVu Medical Technology Co., Ltd.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:HIH)
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