L&M Ultrascope Life Monitoring Sys. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
L&M Ultrascope Life Monitoring Sys. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
L&M Ultrascope Life Monitoring Sys. has 2 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 2 cleared submissions from 1978 to 1978. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by L&M Ultrascope Life Monitoring Sys. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - L&M Ultrascope Life Monitoring Sys.
2 devices