Mccue Plc is one of 507 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Mccue Plc - FDA 510(k) Cleared Devices
Recent clearances: MCCUE ENERGIST ULTRA VPL INTENSE PULSE LIGHT SYSTEM, MCCUE PLC ENERGIST ULTRA VARIABLE PULSED LIGHT SYSTEM
2
Total
2
Cleared
0
Denied
Mccue Plc has 2 FDA 510(k) cleared medical devices. Based in Southampton, Hampshire, GB.
Historical record: 2 cleared submissions from 2004 to 2006. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Mccue Plc Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Bsi Healthcare as regulatory consultant.
FDA 510(k) Regulatory Record - Mccue Plc
2 devices