FDA 510(k)

Progenix Select 刺激器

K 號：K242460 · 2025-04-02

決定日期2025-04-02

產品代碼NUH

諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

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.

常見問題

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.

相關器械（代碼：NUH）

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器材摘要

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相關器械（代碼：NUH）

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