FDA 510(k)

NerivioInfinity

K号: K232152 · 2023-11-08

决定日期2023-11-08

产品代码QGT

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决定实质等同

器械摘要

NerivioInfinity is the device name listed in this FDA 510(k) record. The listed applicant is Theranica Bioelectronics , Ltd.. It received FDA 510(k) clearance on 2023-11-08 under 510(k) number K232152. The device is classified under product code QGT. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the NerivioInfinity?

NerivioInfinity is a medical device that received FDA 510(k) clearance on 2023-11-08. The listed applicant is Theranica Bioelectronics , Ltd.. The 510(k) number is K232152.

When did NerivioInfinity receive FDA 510(k) clearance?

NerivioInfinity received FDA 510(k) clearance on 2023-11-08, under 510(k) number K232152.

Who is the listed applicant for NerivioInfinity?

The FDA 510(k) record lists Theranica Bioelectronics , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NerivioInfinity?

The FDA product code for NerivioInfinity is QGT.

列明Theranica Bioelectronics , Ltd.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。

K223169Nerivio K203181Nerivio, FGD000075-4.7

官方来源

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