Sway Medical, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Sway Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Tulsa, US.
Latest FDA clearance: Feb 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Sway Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Steurer Consulting Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Sway Medical, Inc.
1 devices