Arjohuntleigh Polska SP Z.O.O. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Arjohuntleigh Polska SP Z.O.O. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Arjohuntleigh Polska SP Z.O.O. has 2 FDA 510(k) cleared medical devices. Based in Cardiff, GB.
Historical record: 2 cleared submissions from 2012 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Arjohuntleigh Polska SP Z.O.O. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arjohuntleigh Polska SP Z.O.O.
2 devices