MIM - Centiloid Scaling
K-Number: K233620 · 2024-05-20
ApplicantMim Software, Inc.
Decision Date2024-05-20
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
MIM - Centiloid Scaling is a medical device manufactured by Mim Software, Inc.. It received FDA 510(k) clearance on 2024-05-20 under approval number K233620. 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 - Centiloid Scaling?
MIM - Centiloid Scaling is a medical device that received FDA 510(k) clearance on 2024-05-20. It is manufactured by Mim Software, Inc.. The 510(k) number is K233620.
When was MIM - Centiloid Scaling approved by the FDA?
MIM - Centiloid Scaling received FDA 510(k) clearance on 2024-05-20, under approval number K233620.
What company makes MIM - Centiloid Scaling?
MIM - Centiloid Scaling is manufactured by Mim Software, Inc..
What is the FDA product code for MIM - Centiloid Scaling?
The FDA product code for MIM - Centiloid Scaling 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.