Stimq, LLC is one of 4820 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stimq, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Stimq, LLC has 1 FDA 510(k) cleared medical devices. Based in Fort Lauderdale, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Stimq, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Stimq, LLC
1 devices