KISS動態後腰支撐，KISS動態實心降座
K 號：K211919 · 2022-03-04
廣告
器材摘要
KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat is the device name listed in this FDA 510(k) record. The listed applicant is Kinetic Innovative Seating System, LLC. It received FDA 510(k) clearance on 2022-03-04 under 510(k) number K211919. The device is classified under product code KNN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat?
KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat is a medical device that received FDA 510(k) clearance on 2022-03-04. The listed applicant is Kinetic Innovative Seating System, LLC. The 510(k) number is K211919.
When did KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat receive FDA 510(k) clearance?
KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat received FDA 510(k) clearance on 2022-03-04, under 510(k) number K211919.
Who is the listed applicant for KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat?
The FDA 510(k) record lists Kinetic Innovative Seating System, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat?
The FDA product code for KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat is KNN.
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