FDA 510(k)

Progenix Select Stim

K号: K242460 · 2025-04-02

决定日期2025-04-02

产品代码NUH

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器械摘要

Progenix Select Stim is the device name listed in this FDA 510(k) record. The listed applicant is Progenix, LLC. It received FDA 510(k) clearance on 2025-04-02 under 510(k) number K242460. 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 Progenix Select Stim?

Progenix Select Stim is a medical device that received FDA 510(k) clearance on 2025-04-02. The listed applicant is Progenix, LLC. The 510(k) number is K242460.

When did Progenix Select Stim receive FDA 510(k) clearance?

Progenix Select Stim received FDA 510(k) clearance on 2025-04-02, under 510(k) number K242460.

Who is the listed applicant for Progenix Select Stim?

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

What is the FDA product code for Progenix Select Stim?

The FDA product code for Progenix Select Stim is NUH.

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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器械摘要

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相关器械（代码：NUH）

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