UNILITH 2 PULSE GENERATORS #7550, 7552, 7760, 7762

UNILITH 2 PULSE GENERATORS #7550, 7552, 7760, 7762 is an FDA 510(k)-cleared medical device (K852973) manufactured by Ela Medical, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on March 30, 1986. Regulation: 8.