Medmark Technologies, LLC is one of 25198 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medmark Technologies, LLC - FDA 510(k) Cleared Devices
Recent clearances: GS-128 GRADIENT COMPRESSION SYSTEM
1
Total
1
Cleared
0
Denied
Medmark Technologies, LLC has 1 FDA 510(k) cleared medical devices. Based in Perkasie, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medmark Technologies, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Medmark Technologies, LLC
1 devices