Collimare, LLC is one of 25142 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Collimare, LLC - FDA 510(k) Cleared Devices
Recent clearances: COLLIMARE COLLIMATOR FAMILY
1
Total
1
Cleared
0
Denied
Collimare, LLC has 1 FDA 510(k) cleared medical devices. Based in Arvada, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Collimare, LLC 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 - Collimare, LLC
1 devices