CVS Health 干口喷雾，OraLabs 干口喷雾
K号: K181839 · 2019-11-21
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器械摘要
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.
常见问题
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.
相关临床试验
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相关器械（代码：LFD）
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息，请务必参考官方记录。
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