服務醫療CDSS
K 號：K241975 · 2025-03-17
廣告
器材摘要
SERV MEDICAL CDSS is the device name listed in this FDA 510(k) record. The listed applicant is Serv Medical Pte., Ltd.. It received FDA 510(k) clearance on 2025-03-17 under 510(k) number K241975. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the SERV MEDICAL CDSS?
SERV MEDICAL CDSS is a medical device that received FDA 510(k) clearance on 2025-03-17. The listed applicant is Serv Medical Pte., Ltd.. The 510(k) number is K241975.
When did SERV MEDICAL CDSS receive FDA 510(k) clearance?
SERV MEDICAL CDSS received FDA 510(k) clearance on 2025-03-17, under 510(k) number K241975.
Who is the listed applicant for SERV MEDICAL CDSS?
The FDA 510(k) record lists Serv Medical Pte., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SERV MEDICAL CDSS?
The FDA product code for SERV MEDICAL CDSS is LLZ.
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。
相關器械（代碼：LLZ）
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