Imedrix Inc. (Formerly Piitech Inc.) is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Imedrix Inc. (Formerly Piitech Inc.) - FDA 510(k) Cleared Devices
Recent clearances: KardioScreen
1
Total
1
Cleared
0
Denied
Imedrix Inc. (Formerly Piitech Inc.) has 1 FDA 510(k) cleared medical devices. Based in Milpitas, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Imedrix Inc. (Formerly Piitech Inc.) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Imedrix Inc. (Formerly Piitech Inc.)
1 devices