Centarisone, LLC is one of 22865 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Centarisone, LLC - FDA 510(k) Cleared Devices
Recent clearances: CENTARISONE RIS/PACS
1
Total
1
Cleared
0
Denied
Centarisone, LLC has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 1 cleared submissions from 2006 to 2006. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Centarisone, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Centarisone, LLC
1 devices