3880 MRI Patient Monitoring System
K-Number: K172200 · 2017-10-25
Device Summary
Frequently Asked Questions
What is the 3880 MRI Patient Monitoring System?
3880 MRI Patient Monitoring System is a medical device that received FDA 510(k) clearance on 2017-10-25. It is manufactured by Iradimed Corporation. The 510(k) number is K172200.
When was 3880 MRI Patient Monitoring System approved by the FDA?
3880 MRI Patient Monitoring System received FDA 510(k) clearance on 2017-10-25, under approval number K172200.
What company makes 3880 MRI Patient Monitoring System?
3880 MRI Patient Monitoring System is manufactured by Iradimed Corporation.
What is the FDA product code for 3880 MRI Patient Monitoring System?
The FDA product code for 3880 MRI Patient Monitoring System is MWI.
Related Clinical Trials
Related PubMed Literature
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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.