Megine Industries Sdn Bhd - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Megine Industries Sdn Bhd has 2 FDA 510(k) cleared medical devices. Based in Kuala Lumpur, MY.
Last cleared in 2022. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Megine Industries Sdn Bhd Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
2 devices