Hong Kong Etech Groups Limited - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Hong Kong Etech Groups Limited has 1 FDA 510(k) cleared medical devices. Based in Hong Kong, CN.
Latest FDA clearance: Mar 2024. Active since 2024. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Hong Kong Etech Groups Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Feiying Drug & Medical Consulting Technical Service Group as regulatory consultant.
FDA 510(k) Regulatory Record - Hong Kong Etech Groups Limited
1 devices