FDA 510(k)

MIM-Thin Client (mobile)

K-Number: K151913 · 2016-04-25

Decision Date2016-04-25

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

MIM-Thin Client (mobile) is a medical device manufactured by Mim Software, Inc.. It received FDA 510(k) clearance on 2016-04-25 under approval number K151913. 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-Thin Client (mobile)?

MIM-Thin Client (mobile) is a medical device that received FDA 510(k) clearance on 2016-04-25. It is manufactured by Mim Software, Inc.. The 510(k) number is K151913.

When was MIM-Thin Client (mobile) approved by the FDA?

MIM-Thin Client (mobile) received FDA 510(k) clearance on 2016-04-25, under approval number K151913.

What company makes MIM-Thin Client (mobile)?

MIM-Thin Client (mobile) is manufactured by Mim Software, Inc..

What is the FDA product code for MIM-Thin Client (mobile)?

The FDA product code for MIM-Thin Client (mobile) 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.