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FDA 510(k)

MIM – Monte Carlo Dosimetry

K-Number: K232862 · 2024-05-13

ApplicantMim Software, Inc.
Decision Date2024-05-13
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIM – Monte Carlo Dosimetry is a medical device manufactured by Mim Software, Inc.. It received FDA 510(k) clearance on 2024-05-13 under approval number K232862. 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 – Monte Carlo Dosimetry?

MIM – Monte Carlo Dosimetry is a medical device that received FDA 510(k) clearance on 2024-05-13. It is manufactured by Mim Software, Inc.. The 510(k) number is K232862.

When was MIM – Monte Carlo Dosimetry approved by the FDA?

MIM – Monte Carlo Dosimetry received FDA 510(k) clearance on 2024-05-13, under approval number K232862.

What company makes MIM – Monte Carlo Dosimetry?

MIM – Monte Carlo Dosimetry is manufactured by Mim Software, Inc..

What is the FDA product code for MIM – Monte Carlo Dosimetry?

The FDA product code for MIM – Monte Carlo Dosimetry 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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