NIDO嬰兒磁共振成像系統
K 號：K242573 · 2024-12-23
廣告
器材摘要
NIDO Baby Magnetic Resonance Imaging System is the device name listed in this FDA 510(k) record. The listed applicant is Jiangsu Lici Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2024-12-23 under 510(k) number K242573. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the NIDO Baby Magnetic Resonance Imaging System?
NIDO Baby Magnetic Resonance Imaging System is a medical device that received FDA 510(k) clearance on 2024-12-23. The listed applicant is Jiangsu Lici Medical Device Co., Ltd.. The 510(k) number is K242573.
When did NIDO Baby Magnetic Resonance Imaging System receive FDA 510(k) clearance?
NIDO Baby Magnetic Resonance Imaging System received FDA 510(k) clearance on 2024-12-23, under 510(k) number K242573.
Who is the listed applicant for NIDO Baby Magnetic Resonance Imaging System?
The FDA 510(k) record lists Jiangsu Lici Medical Device Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NIDO Baby Magnetic Resonance Imaging System?
The FDA product code for NIDO Baby Magnetic Resonance Imaging System is LNH.
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：LNH）
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。
K261283APERTO Lucent MRI 系統Fujifilm CorporationK261758擁抱視覺新生兒MRI系統Aspect Imaging, Ltd.K260758MAGNETOM Free.Max; MAGNETOM Free.StarSiemens Shenzhen Magnetic Resonance , Ltd.K262622Swoop® 輕便式磁共振成像® 系統Hyperfine, Inc.K254250MagicScan-1.5，綠色MR寧靜1.5TXingaoyi Medical Equipment Co.,LtdK253808空氣偵探 DLGE Medical Systems
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