ScanNav 適應解剖外周神經阻斷
K 號：K232787 · 2023-10-06
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器材摘要
ScanNav Anatomy Peripheral Nerve Block is the device name listed in this FDA 510(k) record. The listed applicant is Intelligent Ultrasound Limited. It received FDA 510(k) clearance on 2023-10-06 under 510(k) number K232787. The device is classified under product code QRG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the ScanNav Anatomy Peripheral Nerve Block?
ScanNav Anatomy Peripheral Nerve Block is a medical device that received FDA 510(k) clearance on 2023-10-06. The listed applicant is Intelligent Ultrasound Limited. The 510(k) number is K232787.
When did ScanNav Anatomy Peripheral Nerve Block receive FDA 510(k) clearance?
ScanNav Anatomy Peripheral Nerve Block received FDA 510(k) clearance on 2023-10-06, under 510(k) number K232787.
Who is the listed applicant for ScanNav Anatomy Peripheral Nerve Block?
The FDA 510(k) record lists Intelligent Ultrasound Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ScanNav Anatomy Peripheral Nerve Block?
The FDA product code for ScanNav Anatomy Peripheral Nerve Block is QRG.
相關臨床試驗
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相關器械（代碼：QRG）
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。
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