LEAD MODELS MUM 1260, MUM 1290

LEAD MODELS MUM 1260, MUM 1290 is an FDA 510(k)-cleared medical device (K790386) 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 April 2, 1979. Regulation: 8.