CathRx, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
CathRx, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Rydalmere, AU.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by CathRx, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acom N Oakes, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - CathRx, Ltd.
1 devices