GuruNanda乾口口腔漱口水及GuruNanda乾口口腔噴劑
K 號:K231205 · 2023-08-22
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器材摘要
常見問題
What is the GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray?
GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray is a medical device that received FDA 510(k) clearance on 2023-08-22. The listed applicant is Gurunanda, LLC. The 510(k) number is K231205.
When did GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray receive FDA 510(k) clearance?
GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray received FDA 510(k) clearance on 2023-08-22, under 510(k) number K231205.
Who is the listed applicant for GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray?
The FDA 510(k) record lists Gurunanda, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray?
The FDA product code for GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray is LFD.
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:LFD)
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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