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FDA 510(k)

Solero 微波组织消融(MTA)系统及配件

K号: K223581 · 2023-03-27

决定日期2023-03-27
产品代码NEY
咨询委员会SU 请注意,您提供的文本“SU”不足以进行翻译。请提供完整的描述性文本以便进行翻译。
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器械摘要

Solero Microwave Tissue Ablation (MTA) System and Accessories is the device name listed in this FDA 510(k) record. The listed applicant is AngioDynamics, Inc.. It received FDA 510(k) clearance on 2023-03-27 under 510(k) number K223581. The device is classified under product code NEY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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

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列明AngioDynamics, Inc.为申报人的其他记录

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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

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