Modulated Imaging, Inc. is one of 18017 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Modulated Imaging, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Clarifi Imaging System, Ox-Imager CS
2
Total
2
Cleared
0
Denied
Modulated Imaging, Inc. has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 2 cleared submissions from 2016 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Modulated Imaging, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by O'Connell Regulatory Consultants, Inc. and O’Connell Regulatory Consultants, Inc.. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Modulated Imaging, Inc.
2 devices