Biomedical Life Systems is one of 25742 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomedical Life Systems - FDA 510(k) Cleared Devices
Recent clearances: ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-2, ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3
2
Total
2
Cleared
0
Denied
Biomedical Life Systems has 2 FDA 510(k) cleared medical devices. Based in Vista, US.
Historical record: 2 cleared submissions from 2003 to 2003. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Biomedical Life Systems Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biomedical Life Systems
2 devices