MOR
K 號：K241897 · 2025-02-11
廣告
器材摘要
MOR is the device name listed in this FDA 510(k) record. The listed applicant is Morari, Inc.. It received FDA 510(k) clearance on 2025-02-11 under 510(k) number K241897. The device is classified under product code QRC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the MOR?
MOR is a medical device that received FDA 510(k) clearance on 2025-02-11. The listed applicant is Morari, Inc.. The 510(k) number is K241897.
When did MOR receive FDA 510(k) clearance?
MOR received FDA 510(k) clearance on 2025-02-11, under 510(k) number K241897.
Who is the listed applicant for MOR?
The FDA 510(k) record lists Morari, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MOR?
The FDA product code for MOR is QRC.
相關 PubMed 文獻
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：QRC）
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