Solero 微波组织消融(MTA)系统及配件
K号: K223581 · 2023-03-27
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器械摘要
常见问题
What is the Solero Microwave Tissue Ablation (MTA) System and Accessories?
Solero Microwave Tissue Ablation (MTA) System and Accessories is a medical device that received FDA 510(k) clearance on 2023-03-27. The listed applicant is AngioDynamics, Inc.. The 510(k) number is K223581.
When did Solero Microwave Tissue Ablation (MTA) System and Accessories receive FDA 510(k) clearance?
Solero Microwave Tissue Ablation (MTA) System and Accessories received FDA 510(k) clearance on 2023-03-27, under 510(k) number K223581.
Who is the listed applicant for Solero Microwave Tissue Ablation (MTA) System and Accessories?
The FDA 510(k) record lists AngioDynamics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Solero Microwave Tissue Ablation (MTA) System and Accessories?
The FDA product code for Solero Microwave Tissue Ablation (MTA) System and Accessories is NEY.
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。
列明AngioDynamics, Inc.为申报人的其他记录
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:NEY)
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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