Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by IRADIMED CORPORATION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K172200
07/21/2017
3880 MRI Patient Monitoring System
Iradimed Corporation
K090087
01/13/2009
MRIDIUM 3860 MRI INFUSION PUMP/MONITORING SYSTEM
IRADIMED CORPORATION
K050301
02/08/2005
MRIDIUM 3850 MRI PUMP SYSTEM
IRADIMED CORPORATION
K143369
11/25/2014
MRidium 3860+ MRI infusion Pump/ Monitoring System
IRADIMED CORPORATION
K180903
04/06/2018
3880 MRI Patient Monitoring System
Iradimed Corporation
K182900
10/16/2018
3880 MRI Patient Monitoring System
Iradimed Corporation
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact