Tournicare Pty, Ltd. is one of 142 FDA 510(k) medical device manufacturers from Australia in the dataset, ranked by real submission volume.
Tournicare Pty, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Tournicare ARMA Automatic Blood Pressure Monitor (ARMA-08)
1
Total
1
Cleared
0
Denied
Tournicare Pty, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Balwyn, AU.
Latest FDA clearance: Jun 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Tournicare Pty, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Donawa Lifescience as regulatory consultant.
FDA 510(k) Regulatory Record - Tournicare Pty, Ltd.
1 devices