BURRON MICROCATH INTRA. CATH. PLACEMENTT

BURRON MICROCATH INTRA. CATH. PLACEMENTT is an FDA 510(k)-cleared medical device (K801941) manufactured by Burron Medical Products, 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 August 26, 1980. Regulation: 8.