MILL-ROSE PERCUTANEOUS PROCEDURAL KIT

MILL-ROSE PERCUTANEOUS PROCEDURAL KIT is an FDA 510(k)-cleared medical device (K935858) manufactured by Mill-Rose Laboratory. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 21, 1994. Regulation: 8.