Monitor/Demlar is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Monitor/Demlar - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Monitor/Demlar has 1 FDA 510(k) cleared medical devices. Based in Hillsborough, US.
Historical record: 1 cleared submissions from 1989 to 1989. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Monitor/Demlar Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Monitor/Demlar
1 devices