Plastikon Industries - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Plastikon Industries has 1 FDA 510(k) cleared medical devices. Based in Hayward, US.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Plastikon Industries Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hantel Technologies, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Plastikon Industries
1 devices