Novitas Medical, LLC is one of 20549 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Novitas Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: COPRESSION SYSTEMS (MODELS CMP-001 AND CMP-002)
1
Total
1
Cleared
0
Denied
Novitas Medical, LLC has 1 FDA 510(k) cleared medical devices. Based in Brea, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Novitas Medical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Novitas Medical, LLC
1 devices