Hydris® 口腔冲洗剂
K号: K163029 · 2017-06-19
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器械摘要
Hydris™ Oral Rinse is the device name listed in this FDA 510(k) record. The listed applicant is Biopharm Consult, LLC. It received FDA 510(k) clearance on 2017-06-19 under 510(k) number K163029. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.
常见问题
What is the Hydris™ Oral Rinse?
Hydris™ Oral Rinse is a medical device that received FDA 510(k) clearance on 2017-06-19. The listed applicant is Biopharm Consult, LLC. The 510(k) number is K163029.
When did Hydris™ Oral Rinse receive FDA 510(k) clearance?
Hydris™ Oral Rinse received FDA 510(k) clearance on 2017-06-19, under 510(k) number K163029.
Who is the listed applicant for Hydris™ Oral Rinse?
The FDA 510(k) record lists Biopharm Consult, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Hydris™ Oral Rinse?
The FDA product code for Hydris™ Oral 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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