CVS Health乾口噴劑，OraLabs乾口噴劑
K 號：K181839 · 2019-11-21
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器材摘要
CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray is the device name listed in this FDA 510(k) record. The listed applicant is Oralabs, Inc.. It received FDA 510(k) clearance on 2019-11-21 under 510(k) number K181839. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.
常見問題
What is the CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray?
CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray is a medical device that received FDA 510(k) clearance on 2019-11-21. The listed applicant is Oralabs, Inc.. The 510(k) number is K181839.
When did CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray receive FDA 510(k) clearance?
CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray received FDA 510(k) clearance on 2019-11-21, under 510(k) number K181839.
Who is the listed applicant for CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray?
The FDA 510(k) record lists Oralabs, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CVS Health Dry Mouth Spray, OraLabs Dry Mouth Spray?
The FDA product code for CVS Health Dry Mouth Spray, OraLabs Dry Mouth 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
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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