CloSYS®干口敏感漱口水
K号: K250390 · 2025-05-19
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器械摘要
CloSYS® Dry Mouth Sensitive Mouth Rinse is the device name listed in this FDA 510(k) record. The listed applicant is Rowpar Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 2025-05-19 under 510(k) number K250390. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.
常见问题
What is the CloSYS® Dry Mouth Sensitive Mouth Rinse?
CloSYS® Dry Mouth Sensitive Mouth Rinse is a medical device that received FDA 510(k) clearance on 2025-05-19. The listed applicant is Rowpar Pharmaceuticals, Inc.. The 510(k) number is K250390.
When did CloSYS® Dry Mouth Sensitive Mouth Rinse receive FDA 510(k) clearance?
CloSYS® Dry Mouth Sensitive Mouth Rinse received FDA 510(k) clearance on 2025-05-19, under 510(k) number K250390.
Who is the listed applicant for CloSYS® Dry Mouth Sensitive Mouth Rinse?
The FDA 510(k) record lists Rowpar Pharmaceuticals, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CloSYS® Dry Mouth Sensitive Mouth Rinse?
The FDA product code for CloSYS® Dry Mouth Sensitive Mouth Rinse 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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