ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC.

ELECTRODE SEMI-FLOTATION CATHETER BY J-LLOYD MEDICAL, INC. is an FDA 510(k)-cleared medical device (K973639) manufactured by J-Lloyd Medical, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 19, 1998. Regulation: 8.