Interlab(Electromechanical) is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Interlab(Electromechanical) - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Interlab(Electromechanical) has 1 FDA 510(k) cleared medical devices. Based in London,Nw11 8nd, England, GB.
Historical record: 1 cleared submissions from 1985 to 1985. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Interlab(Electromechanical) Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Interlab(Electromechanical)
1 devices