DYNABITE CARDIOVASCULAR BIOPSY FORCEPS

DYNABITE CARDIOVASCULAR BIOPSY FORCEPS is an FDA 510(k)-cleared medical device (K951447) manufactured by Portlyn Corp.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 26, 1995. Regulation: 8.