Vesseal
K号: K221280 · 2022-12-09
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决定日期2022-12-09
产品代码GAW
咨询委员会SU
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决定实质等同
器械摘要
Vesseal is the device name listed in this FDA 510(k) record. The listed applicant is Lydus Medical , Ltd.. It received FDA 510(k) clearance on 2022-12-09 under 510(k) number K221280. The device is classified under product code GAW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
常见问题
What is the Vesseal?
Vesseal is a medical device that received FDA 510(k) clearance on 2022-12-09. The listed applicant is Lydus Medical , Ltd.. The 510(k) number is K221280.
When did Vesseal receive FDA 510(k) clearance?
Vesseal received FDA 510(k) clearance on 2022-12-09, under 510(k) number K221280.
Who is the listed applicant for Vesseal?
The FDA 510(k) record lists Lydus Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Vesseal?
The FDA product code for Vesseal is GAW.
相关临床试验
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相关器械（代码：GAW）
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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