PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM

PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM is an FDA 510(k)-cleared medical device (K962226) manufactured by Johnson & Johnson 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 22, 1996. Regulation: 8.