Bromac Assistive Technology is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bromac Assistive Technology - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Bromac Assistive Technology has 2 FDA 510(k) cleared medical devices. Based in Lancaster, US.
Historical record: 2 cleared submissions from 2001 to 2002. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Bromac Assistive Technology Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bromac Assistive Technology
2 devices