Biotab, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Biotab, LLC has 1 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Biotab, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
1 devices