10 AND 12 FRENCH VESSEL DILATORS

10 AND 12 FRENCH VESSEL DILATORS is an FDA 510(k)-cleared medical device (K874738) manufactured by Impra, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 1, 1988. Regulation: 8.