DBB-06 PRO 血液透析输送系统 (DBB-06 PRO)
K号: K242155 · 2025-05-15
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器械摘要
常见问题
What is the DBB-06 PRO Hemodialysis Delivery System (DBB-06 PRO)?
DBB-06 PRO Hemodialysis Delivery System (DBB-06 PRO) is a medical device that received FDA 510(k) clearance on 2025-05-15. The listed applicant is NIKKISO CO., LTD.. The 510(k) number is K242155.
When did DBB-06 PRO Hemodialysis Delivery System (DBB-06 PRO) receive FDA 510(k) clearance?
DBB-06 PRO Hemodialysis Delivery System (DBB-06 PRO) received FDA 510(k) clearance on 2025-05-15, under 510(k) number K242155.
Who is the listed applicant for DBB-06 PRO Hemodialysis Delivery System (DBB-06 PRO)?
The FDA 510(k) record lists NIKKISO CO., LTD. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DBB-06 PRO Hemodialysis Delivery System (DBB-06 PRO)?
The FDA product code for DBB-06 PRO Hemodialysis Delivery System (DBB-06 PRO) is KDI.
相关临床试验
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列明NIKKISO 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:KDI)
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。
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