Velox Manufacturing, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Velox Manufacturing, Inc. has 1 FDA 510(k) cleared medical devices. Based in Langley, CA.
Latest FDA clearance: Jan 2024. Active since 2024. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Velox Manufacturing, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Velox Manufacturing, Inc.
1 devices