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FDA 510(k)

MIM – LesionID Pro

K-Number: K251883 · 2025-12-11

ApplicantMim Software, Inc.
Decision Date2025-12-11
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIM – LesionID Pro is a medical device manufactured by Mim Software, Inc.. It received FDA 510(k) clearance on 2025-12-11 under approval number K251883. 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 MIM – LesionID Pro?

MIM – LesionID Pro is a medical device that received FDA 510(k) clearance on 2025-12-11. It is manufactured by Mim Software, Inc.. The 510(k) number is K251883.

When was MIM – LesionID Pro approved by the FDA?

MIM – LesionID Pro received FDA 510(k) clearance on 2025-12-11, under approval number K251883.

What company makes MIM – LesionID Pro?

MIM – LesionID Pro is manufactured by Mim Software, Inc..

What is the FDA product code for MIM – LesionID Pro?

The FDA product code for MIM – LesionID Pro is LLZ.

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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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