LacriPro Punctum Plug
K号: K161673 · 2016-11-18
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器械摘要
LacriPro Punctum Plug is the device name listed in this FDA 510(k) record. The listed applicant is Lacrimedics, Inc.. It received FDA 510(k) clearance on 2016-11-18 under 510(k) number K161673. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.
常见问题
What is the LacriPro Punctum Plug?
LacriPro Punctum Plug is a medical device that received FDA 510(k) clearance on 2016-11-18. The listed applicant is Lacrimedics, Inc.. The 510(k) number is K161673.
When did LacriPro Punctum Plug receive FDA 510(k) clearance?
LacriPro Punctum Plug received FDA 510(k) clearance on 2016-11-18, under 510(k) number K161673.
Who is the listed applicant for LacriPro Punctum Plug?
The FDA 510(k) record lists Lacrimedics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LacriPro Punctum Plug?
The FDA product code for LacriPro Punctum Plug 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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