FDA 510(k)

InMode RF 多系统

K号: K201150 · 2020-07-22

决定日期2020-07-22

产品代码GEI

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决定实质等同

器械摘要

InMode RF Multi-System is the device name listed in this FDA 510(k) record. The listed applicant is InMode , Ltd.. It received FDA 510(k) clearance on 2020-07-22 under 510(k) number K201150. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the InMode RF Multi-System?

InMode RF Multi-System is a medical device that received FDA 510(k) clearance on 2020-07-22. The listed applicant is InMode , Ltd.. The 510(k) number is K201150.

When did InMode RF Multi-System receive FDA 510(k) clearance?

InMode RF Multi-System received FDA 510(k) clearance on 2020-07-22, under 510(k) number K201150.

Who is the listed applicant for InMode RF Multi-System?

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

What is the FDA product code for InMode RF Multi-System?

The FDA product code for InMode RF Multi-System is GEI.

列明InMode , 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。

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相关器械（代码：GEI）

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。

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