Therox, Inc. is one of 20340 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Therox, Inc. - FDA 510(k) Cleared Devices
Recent clearances: THEROX INFUSION CATHETER, MODEL INCA-1, THEROX INFUSION GUIDEWIRES
2
Total
2
Cleared
0
Denied
Therox, Inc. has 2 FDA 510(k) cleared medical devices. Based in Irvine, US.
Historical record: 2 cleared submissions from 1997 to 2006. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Therox, Inc. 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 - Therox, Inc.
2 devices