MIM Y90 Dosimetry
K-Number: K172218 · 2017-11-21
ApplicantMim Software, Inc.
Decision Date2017-11-21
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MIM Y90 Dosimetry is a medical device manufactured by Mim Software, Inc.. It received FDA 510(k) clearance on 2017-11-21 under approval number K172218. 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 Y90 Dosimetry?
MIM Y90 Dosimetry is a medical device that received FDA 510(k) clearance on 2017-11-21. It is manufactured by Mim Software, Inc.. The 510(k) number is K172218.
When was MIM Y90 Dosimetry approved by the FDA?
MIM Y90 Dosimetry received FDA 510(k) clearance on 2017-11-21, under approval number K172218.
What company makes MIM Y90 Dosimetry?
MIM Y90 Dosimetry is manufactured by Mim Software, Inc..
What is the FDA product code for MIM Y90 Dosimetry?
The FDA product code for MIM Y90 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.