CLINICATH POLYFLOW POLYURETHANE PERIPHERALLY INSERTED CATHETERS

CLINICATH POLYFLOW POLYURETHANE PERIPHERALLY INSERTED CATHETERS is an FDA 510(k)-cleared medical device (K984055) manufactured by Sims Deltec, 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 January 28, 1999. Regulation: 8.