NDOHD 高解析度影像系統（NDOHD）
K 號：K190420 · 2019-04-15
廣告
器材摘要
NDOHD High Definition Imaging System (NDOHD) is the device name listed in this FDA 510(k) record. The listed applicant is Altaravision, Inc.. It received FDA 510(k) clearance on 2019-04-15 under 510(k) number K190420. 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 NDOHD High Definition Imaging System (NDOHD)?
NDOHD High Definition Imaging System (NDOHD) is a medical device that received FDA 510(k) clearance on 2019-04-15. The listed applicant is Altaravision, Inc.. The 510(k) number is K190420.
When did NDOHD High Definition Imaging System (NDOHD) receive FDA 510(k) clearance?
NDOHD High Definition Imaging System (NDOHD) received FDA 510(k) clearance on 2019-04-15, under 510(k) number K190420.
Who is the listed applicant for NDOHD High Definition Imaging System (NDOHD)?
The FDA 510(k) record lists Altaravision, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NDOHD High Definition Imaging System (NDOHD)?
The FDA product code for NDOHD High Definition Imaging System (NDOHD) 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