AITRICS-VC
K 號:K240756 · 2024-07-23
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器材摘要
AITRICS-VC is the device name listed in this FDA 510(k) record. The listed applicant is Aitrics Co., Ltd.. It received FDA 510(k) clearance on 2024-07-23 under 510(k) number K240756. The device is classified under product code PLB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the AITRICS-VC?
AITRICS-VC is a medical device that received FDA 510(k) clearance on 2024-07-23. The listed applicant is Aitrics Co., Ltd.. The 510(k) number is K240756.
When did AITRICS-VC receive FDA 510(k) clearance?
AITRICS-VC received FDA 510(k) clearance on 2024-07-23, under 510(k) number K240756.
Who is the listed applicant for AITRICS-VC?
The FDA 510(k) record lists Aitrics Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AITRICS-VC?
The FDA product code for AITRICS-VC is PLB.
相關臨床試驗
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相關器械(代碼:PLB)
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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