MODEL 230-05 CYBERLITH I BIPOL. PULSE G.

MODEL 230-05 CYBERLITH I BIPOL. PULSE G. is an FDA 510(k)-cleared medical device (K810800) manufactured by Intermedics, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on April 30, 1981. Regulation: 8.