Medtronic Advanced Energy, LLC - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Medtronic Advanced Energy, LLC has 3 FDA 510(k) cleared medical devices. Based in Portsmouth, US.
Historical record: 3 cleared submissions from 2012 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medtronic Advanced Energy, LLC Filter by specialty or product code using the sidebar.
3 devices
Cleared
Dec 03, 2013
AQUAMANTYS 2.3 BIPOLAR SEALER, EVS 4.0 EPIDURAL VEIN SEALER, MINI EVS 3.4...
General & Plastic Surgery
71d
Cleared
Jan 10, 2013
AQUAMANTYS ENDO DBS 8.7 DISSECTING BIPOLAR SEALER
General & Plastic Surgery
90d
Cleared
Nov 02, 2012
EC 2.7 ENDOSCOPIC CUTTER
General & Plastic Surgery
221d