Lamont Medical, Inc. is one of 10971 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lamont Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: WARATAH DIGITAL EEG AND SLEEP ACQUISITION DEVICES WITH, OR WITHOUT, PULSE OXIMETRY,CARDINAL DIGITAL EEG AND SLEEP ACQUIS
2
Total
2
Cleared
0
Denied
Lamont Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in Stoughton, US.
Historical record: 2 cleared submissions from 1999 to 2004. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Lamont Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lamont Medical, Inc.
2 devices