Martin D. Lerman is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Martin D. Lerman - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Martin D. Lerman has 1 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 1 cleared submissions from 1983 to 1983. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Martin D. Lerman Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Martin D. Lerman
1 devices