P.K. Morgan , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
P.K. Morgan , Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
P.K. Morgan , Ltd. has 4 FDA 510(k) cleared medical devices. Based in Kent Rainham Me8 7ed, GB.
Historical record: 4 cleared submissions from 1996 to 1997. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by P.K. Morgan , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - P.K. Morgan , Ltd.
4 devices