Pragonix Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pragonix Technologies - FDA 510(k) Cleared Devices
Recent clearances: SherpaPak Lung Preservation System , SherpaPak Liver Transport System
1
Total
0
Cleared
0
Denied
Pragonix Technologies has 0 FDA 510(k) cleared medical devices. Based in Braintree, US.
Historical record: 0 cleared submissions from 2020 to 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Pragonix Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Northstar Biomedical Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Pragonix Technologies
1 devices