泪液池可溶解的泪点塞
K号: K190210 · 2019-10-24
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器械摘要
Tear Pool Dissolvable Punctum Plugs is the device name listed in this FDA 510(k) record. The listed applicant is Alphamed, Inc.. It received FDA 510(k) clearance on 2019-10-24 under 510(k) number K190210. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.
常见问题
What is the Tear Pool Dissolvable Punctum Plugs?
Tear Pool Dissolvable Punctum Plugs is a medical device that received FDA 510(k) clearance on 2019-10-24. The listed applicant is Alphamed, Inc.. The 510(k) number is K190210.
When did Tear Pool Dissolvable Punctum Plugs receive FDA 510(k) clearance?
Tear Pool Dissolvable Punctum Plugs received FDA 510(k) clearance on 2019-10-24, under 510(k) number K190210.
Who is the listed applicant for Tear Pool Dissolvable Punctum Plugs?
The FDA 510(k) record lists Alphamed, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Tear Pool Dissolvable Punctum Plugs?
The FDA product code for Tear Pool Dissolvable Punctum Plugs is LZU.
相关临床试验
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相关器械（代码：LZU）
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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