Well Lead Medical Instruments - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Well Lead Medical Instruments has 4 FDA 510(k) cleared medical devices. Based in Apollo Beach, US.
Historical record: 4 cleared submissions from 2005 to 2008. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Well Lead Medical Instruments Filter by specialty or product code using the sidebar.
4 devices
Cleared
Oct 08, 2008
WELL LEAD SILICONE AND LATEX FOLEY CATHETERS
Gastroenterology & Urology
13d
Cleared
Jul 10, 2008
WELL LEAD REINFORCED ENDOTRACHEAL TUBE
Anesthesiology
220d
Cleared
Feb 18, 2005
WELL LEAD ENDOTRACHEAL TUBE
Anesthesiology
142d
Cleared
Feb 17, 2005
WELL LEAD TRACHEOSTOMY TUBE
Anesthesiology
141d