Pegabus Egerton, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Pegabus Egerton, Ltd. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Pegabus Egerton, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Kent Br1 3tu, GB.
Historical record: 2 cleared submissions from 1995 to 1995. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pegabus Egerton, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pegabus Egerton, Ltd.
2 devices