维斯安医疗胆管塞
K号: K222164 · 2022-12-23
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器械摘要
Visant Medical Canalicular Plug is the device name listed in this FDA 510(k) record. The listed applicant is Visant Medical, Inc.. It received FDA 510(k) clearance on 2022-12-23 under 510(k) number K222164. The device is classified under product code LZU. FDA Decision: Substantially Equivalent.
常见问题
What is the Visant Medical Canalicular Plug?
Visant Medical Canalicular Plug is a medical device that received FDA 510(k) clearance on 2022-12-23. The listed applicant is Visant Medical, Inc.. The 510(k) number is K222164.
When did Visant Medical Canalicular Plug receive FDA 510(k) clearance?
Visant Medical Canalicular Plug received FDA 510(k) clearance on 2022-12-23, under 510(k) number K222164.
Who is the listed applicant for Visant Medical Canalicular Plug?
The FDA 510(k) record lists Visant Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Visant Medical Canalicular Plug?
The FDA product code for Visant Medical Canalicular Plug is LZU.
相关临床试验
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。
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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