MEHIGAN-PILLING PHLEBETOME TM

MEHIGAN-PILLING PHLEBETOME TM is an FDA 510(k)-cleared medical device (K911100) manufactured by Pilling Co.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 20, 1991. Regulation: 8.