IASIS i2 放鬆神經回饋系統
K 號：K252923 · 2026-03-13
廣告
器材摘要
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.
常見問題
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.
相關臨床試驗
相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
廣告