POSSIS MEDICAL MYOPORE BIPOLAR SUTURELESS MYCARDIA

POSSIS MEDICAL MYOPORE BIPOLAR SUTURELESS MYCARDIA is an FDA 510(k)-cleared medical device (K925099) manufactured by Possis Medical, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class III (Premarket Approval) — highest risk category. FDA clearance granted on June 21, 1993. Regulation: 8.