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FDA 510(k)

AIM (N/A)

K-Number: K240937 · 2024-12-16

ApplicantInventeur, LLC
Decision Date2024-12-16
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

What is the AIM (N/A)?

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

When was AIM (N/A) approved by the FDA?

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

What company makes AIM (N/A)?

AIM (N/A) is manufactured by Inventeur, LLC.

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

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

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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