Netech Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Netech Corporation - FDA 510(k) Cleared Devices
Recent clearances: Delta 3300
1
Total
1
Cleared
0
Denied
Netech Corporation has 1 FDA 510(k) cleared medical devices. Based in Farmingdale, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Netech Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Brij Strategic Consultations, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Netech Corporation
1 devices