FDA 510(k)

AIM (N/A)

K 號：K240937 · 2024-12-16

決定日期2024-12-16

產品代碼CCK

諮詢委員會AN

決定相當於

器材摘要

AIM (N/A) is the device name listed in this FDA 510(k) record. The listed applicant is Inventeur, LLC. It received FDA 510(k) clearance on 2024-12-16 under 510(k) number K240937. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the AIM (N/A)?

AIM (N/A) is a medical device that received FDA 510(k) clearance on 2024-12-16. The listed applicant is Inventeur, LLC. The 510(k) number is K240937.

When did AIM (N/A) receive FDA 510(k) clearance?

AIM (N/A) received FDA 510(k) clearance on 2024-12-16, under 510(k) number K240937.

Who is the listed applicant for AIM (N/A)?

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

What is the FDA product code for AIM (N/A)?

The FDA product code for AIM (N/A) is CCK.

相關器械（代碼：CCK）

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官方來源

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