Neuvotion NeuStim NN-01
K 號：K240632 · 2024-11-22
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器材摘要
Neuvotion NeuStim NN-01 is the device name listed in this FDA 510(k) record. The listed applicant is Neuvotion, Inc.. It received FDA 510(k) clearance on 2024-11-22 under 510(k) number K240632. The device is classified under product code GZI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Neuvotion NeuStim NN-01?
Neuvotion NeuStim NN-01 is a medical device that received FDA 510(k) clearance on 2024-11-22. The listed applicant is Neuvotion, Inc.. The 510(k) number is K240632.
When did Neuvotion NeuStim NN-01 receive FDA 510(k) clearance?
Neuvotion NeuStim NN-01 received FDA 510(k) clearance on 2024-11-22, under 510(k) number K240632.
Who is the listed applicant for Neuvotion NeuStim NN-01?
The FDA 510(k) record lists Neuvotion, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Neuvotion NeuStim NN-01?
The FDA product code for Neuvotion NeuStim NN-01 is GZI.
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相關器械（代碼：GZI）
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
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