Primary Technology, LLC is one of 25323 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Primary Technology, LLC - FDA 510(k) Cleared Devices
Recent clearances: SPECTRAPULSE, SPECTRAPULSE
2
Total
2
Cleared
0
Denied
Primary Technology, LLC has 2 FDA 510(k) cleared medical devices. Based in Tampa, US.
Historical record: 2 cleared submissions from 2002 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Primary Technology, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Primary Technology, LLC
2 devices