Kimberly-Clark Corporation
KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS
SKU K113333UPC BTR
In Stock
—
IIFDA 510(k) Cleared (K113333)
1
Free shipping on orders over $99 · 30-day returns
Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human
Kimberly-Clark Corporation
Free shipping on orders over $99 · 30-day returns
KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS is an FDA 510(k)-cleared medical device (K113333) manufactured by Kimberly-Clark Corporation. This device is classified under the Anesthesiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 10, 2012. Regulation: 8.
