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FDA 510(k)

GuruNanda乾口口腔漱口水及GuruNanda乾口口腔噴劑

K 號:K231205 · 2023-08-22

決定日期2023-08-22
產品代碼LFD
決定相當於

器材摘要

GuruNanda Dry Mouth Oral Rinse and GuruNanda Dry Mouth Oral Spray is the device name listed in this FDA 510(k) record. The listed applicant is Gurunanda, LLC. It received FDA 510(k) clearance on 2023-08-22 under 510(k) number K231205. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

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

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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

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