FDA 510(k)

ManaFlexx 2（型号：MF002-RX，MF002-OTC）

K号: K231569 · 2023-11-03

决定日期2023-11-03

产品代码NUH

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决定实质等同

器械摘要

ManaFlexx 2 (model: MF002-RX, MF002-OTC) is the device name listed in this FDA 510(k) record. The listed applicant is Manamed, Inc.. It received FDA 510(k) clearance on 2023-11-03 under 510(k) number K231569. The device is classified under product code NUH. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the ManaFlexx 2 (model: MF002-RX, MF002-OTC)?

ManaFlexx 2 (model: MF002-RX, MF002-OTC) is a medical device that received FDA 510(k) clearance on 2023-11-03. The listed applicant is Manamed, Inc.. The 510(k) number is K231569.

When did ManaFlexx 2 (model: MF002-RX, MF002-OTC) receive FDA 510(k) clearance?

ManaFlexx 2 (model: MF002-RX, MF002-OTC) received FDA 510(k) clearance on 2023-11-03, under 510(k) number K231569.

Who is the listed applicant for ManaFlexx 2 (model: MF002-RX, MF002-OTC)?

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

What is the FDA product code for ManaFlexx 2 (model: MF002-RX, MF002-OTC)?

The FDA product code for ManaFlexx 2 (model: MF002-RX, MF002-OTC) is NUH.

列明Manamed, 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。

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相关器械（代码：NUH）

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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官方来源

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