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FDA 510(k)

MIM-Thin Client (mobile)

K-Number: K151913 · 2016-04-25

ApplicantMim Software, Inc.
Decision Date2016-04-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MIM-Thin Client (mobile) is the device name listed in this FDA 510(k) record. The listed applicant is Mim Software, Inc.. It received FDA 510(k) clearance on 2016-04-25 under 510(k) 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. The listed applicant is Mim Software, Inc.. The 510(k) number is K151913.

When did MIM-Thin Client (mobile) receive FDA 510(k) clearance?

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

Who is the listed applicant for MIM-Thin Client (mobile)?

The FDA 510(k) record lists Mim Software, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

Other records listing Mim Software, Inc. as applicant

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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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