FDA 510(k)

Oral-B乾口口腔噴劑

K 號：K203567 · 2021-04-05

決定日期2021-04-05

產品代碼LFD

決定相當於

器材摘要

Oral-B Dry Mouth Oral Rinse is the device name listed in this FDA 510(k) record. The listed applicant is The Procter & Gamble Company. It received FDA 510(k) clearance on 2021-04-05 under 510(k) number K203567. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

常見問題

What is the Oral-B Dry Mouth Oral Rinse?

Oral-B Dry Mouth Oral Rinse is a medical device that received FDA 510(k) clearance on 2021-04-05. The listed applicant is The Procter & Gamble Company. The 510(k) number is K203567.

When did Oral-B Dry Mouth Oral Rinse receive FDA 510(k) clearance?

Oral-B Dry Mouth Oral Rinse received FDA 510(k) clearance on 2021-04-05, under 510(k) number K203567.

Who is the listed applicant for Oral-B Dry Mouth Oral Rinse?

The FDA 510(k) record lists The Procter & Gamble Company as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Oral-B Dry Mouth Oral Rinse?

The FDA product code for Oral-B Dry Mouth Oral Rinse is LFD.

其他以 The Procter & Gamble Company 為申請人之記錄

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。

K201277Oral-B乾口口腔噴劑 K200881Oral-B iO 測試駕駛功率牙刷試用方案組

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。

K253778Allday 湿潤漱口水Elevate Oral Care K250390CloSYS®乾口敏感口腔噴劑Rowpar Pharmaceuticals, Inc.K240508Salivea乾口異常保濕膠（乾口異常保濕膠）Laclede, Inc.K234015Caphosol®人工唾液（32劑包裝盒）Eusa Pharma (Uk) Limited K231205GuruNanda乾口口腔漱口水及GuruNanda乾口口腔噴劑Gurunanda, LLC K202689Dentilube噴霧Oxy2plus, LLC

官方來源

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