KENDALL SAFETRAK COMBINED EPIDURAL/SPINAL KIT

KENDALL SAFETRAK COMBINED EPIDURAL/SPINAL KIT is an FDA 510(k)-cleared medical device (K941493) manufactured by Kendall Healthcare Products Co. Div.Of Tyco Health. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 21, 1994. Regulation: 8.