IASIS i2放松神经反馈系统
K号: K252923 · 2026-03-13
广告
器械摘要
IASIS i2 Relaxation Neurofeedback System is the device name listed in this FDA 510(k) record. The listed applicant is Iasis Technologies. It received FDA 510(k) clearance on 2026-03-13 under 510(k) number K252923. FDA Decision: Substantially Equivalent.
常见问题
What is the IASIS i2 Relaxation Neurofeedback System?
IASIS i2 Relaxation Neurofeedback System is a medical device that received FDA 510(k) clearance on 2026-03-13. The listed applicant is Iasis Technologies. The 510(k) number is K252923.
When did IASIS i2 Relaxation Neurofeedback System receive FDA 510(k) clearance?
IASIS i2 Relaxation Neurofeedback System received FDA 510(k) clearance on 2026-03-13, under 510(k) number K252923.
Who is the listed applicant for IASIS i2 Relaxation Neurofeedback System?
The FDA 510(k) record lists Iasis Technologies as the applicant. This does not by itself establish the device manufacturer.
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。
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