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FDA 510(k)

MIM – Additional Tracers

K-Number: K223800 · 2023-01-17

Decision Date2023-01-17
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIM – Additional Tracers is a medical device manufactured by Mim Software, Inc.. It received FDA 510(k) clearance on 2023-01-17 under approval number K223800. 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 – Additional Tracers?

MIM – Additional Tracers is a medical device that received FDA 510(k) clearance on 2023-01-17. It is manufactured by Mim Software, Inc.. The 510(k) number is K223800.

When was MIM – Additional Tracers approved by the FDA?

MIM – Additional Tracers received FDA 510(k) clearance on 2023-01-17, under approval number K223800.

What company makes MIM – Additional Tracers?

MIM – Additional Tracers is manufactured by Mim Software, Inc..

What is the FDA product code for MIM – Additional Tracers?

The FDA product code for MIM – Additional Tracers is LLZ.

Other Devices by Mim Software, Inc.

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Related Devices (Code: LLZ)

Official Source

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