FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER

FOOTPRINT MEDICAL PERIPHERALLY INSERTED CENTRAL CATHETER is an FDA 510(k)-cleared medical device (K093252) manufactured by Footprint Medical, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 16, 2009. Regulation: 8.