MIM - MRT Dosimetry
K-Number: K182624 · 2018-12-18
ApplicantMim Software, Inc.
Decision Date2018-12-18
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MIM - MRT Dosimetry is a medical device manufactured by Mim Software, Inc.. It received FDA 510(k) clearance on 2018-12-18 under approval number K182624. 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 - MRT Dosimetry?
MIM - MRT Dosimetry is a medical device that received FDA 510(k) clearance on 2018-12-18. It is manufactured by Mim Software, Inc.. The 510(k) number is K182624.
When was MIM - MRT Dosimetry approved by the FDA?
MIM - MRT Dosimetry received FDA 510(k) clearance on 2018-12-18, under approval number K182624.
What company makes MIM - MRT Dosimetry?
MIM - MRT Dosimetry is manufactured by Mim Software, Inc..
What is the FDA product code for MIM - MRT Dosimetry?
The FDA product code for MIM - MRT Dosimetry is LLZ.
Other Devices by Mim Software, Inc.
Related Devices (Code: LLZ)
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.