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FDA 510(k)

MIM – Dose Analysis

K-Number: K232514 · 2024-05-06

ApplicantMim Software, Inc.
Decision Date2024-05-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIM – Dose Analysis is a medical device manufactured by Mim Software, Inc.. It received FDA 510(k) clearance on 2024-05-06 under approval number K232514. 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 – Dose Analysis?

MIM – Dose Analysis is a medical device that received FDA 510(k) clearance on 2024-05-06. It is manufactured by Mim Software, Inc.. The 510(k) number is K232514.

When was MIM – Dose Analysis approved by the FDA?

MIM – Dose Analysis received FDA 510(k) clearance on 2024-05-06, under approval number K232514.

What company makes MIM – Dose Analysis?

MIM – Dose Analysis is manufactured by Mim Software, Inc..

What is the FDA product code for MIM – Dose Analysis?

The FDA product code for MIM – Dose Analysis 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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