PUNCTURE KIT, INTERNAL JUGULAR

PUNCTURE KIT, INTERNAL JUGULAR is an FDA 510(k)-cleared medical device (K770462) manufactured by Arrow Intl., 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 March 13, 1977. Regulation: 8.