Imacor, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Imacor, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ImaCor Zura Handheld ZHH-010
3
Total
3
Cleared
0
Denied
Imacor, Inc. has 3 FDA 510(k) cleared medical devices. Based in Uniondale, US.
Last cleared in 2022. Active since 2010. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Imacor, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Imacor, Inc.
3 devices