Rapidex of London is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Rapidex of London - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Rapidex of London has 1 FDA 510(k) cleared medical devices. Based in Richmond, Surrey, GB.
Historical record: 1 cleared submissions from 1987 to 1987. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Rapidex of London Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rapidex of London
1 devices