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FDA 510(k)

AutoSeg

K-Number: K220039 · 2022-07-20

ApplicantAi Medic, Inc.
Decision Date2022-07-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AutoSeg is a medical device manufactured by Ai Medic, Inc.. It received FDA 510(k) clearance on 2022-07-20 under approval number K220039. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AutoSeg?

AutoSeg is a medical device that received FDA 510(k) clearance on 2022-07-20. It is manufactured by Ai Medic, Inc.. The 510(k) number is K220039.

When was AutoSeg approved by the FDA?

AutoSeg received FDA 510(k) clearance on 2022-07-20, under approval number K220039.

What company makes AutoSeg?

AutoSeg is manufactured by Ai Medic, Inc..

What is the FDA product code for AutoSeg?

The FDA product code for AutoSeg is LLZ.

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Official Source

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